Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 13:113122874 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM025192

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_014162

This variation has 11 HGVS names - click the plus to show

Variation displays