Canonical Allele Identifier: PA2741865013
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2884032
ClinVar RCV Id: RCV003724222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Ala1558Thr
CA5902422
NM_001351295.2:c.4672G>A