Canonical Allele Identifier: PA097149
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Ala1457Thr
CA218407557
NM_000352.6:c.4369G>A