Canonical Allele Identifier: PA2825148510
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Ala1152Val
CA379798305
NM_000352.6:c.3455C>T