Canonical Allele Identifier: PA277375
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 210069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Leu511Pro
CA277373
NM_001287174.3:c.1532T>C