Most severe consequence
13
missense variant
Alleles
T/G
Location
Primary_assembly 2:26948922 (forward strand)|VCF:2 26948922 rs41257509 T G
Evidence status 
HGVS names
This variant has 3 HGVS names - Show
Original source
Short variant data imported from EVA [remapped to ARS-UCD1.3] (release 11/2024)|View in EVA
About this variant
This variant has predicted consequences for 1 transcript.
