Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 7:128254587 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981201

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_011955

This variation has 3 HGVS names - click the plus to show

Variation displays