Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/A/C | Ancestral: T | Ambiguity code: H

Chromosome 7:2554374 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_031202

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 26 transcripts and has 2 sample genotypes.

Variant displays