Canonical Allele Identifier: PA916030858
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 18449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Gly738Val
CA220124
NM_001351295.2:c.2213G>T