Canonical Allele Identifier: PA2827604753
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Ala1152Val
CA379798305
NM_001351296.2:c.3455C>T