Canonical Allele Identifier: PA916031010
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 21169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Gln211Lys
CA341693
NM_001351297.2:c.631C>A