Canonical Allele Identifier: PA916030883
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Ala1174Val
CA379798305
NM_001351295.2:c.3521C>T