Canonical Allele Identifier: PA277374
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 210069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Leu511Pro
CA277373
NM_000352.6:c.1532T>C