Allele Registry

Canonical Allele Identifier: PA2827604937

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV003851783

ClinVar Variation:

2999152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338225.1:p.Ala1369Thr	CA5902584 NM_001351296.2:c.4105G>A