Allele Registry

Canonical Allele Identifier: PA2825148722

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV003851783

ClinVar Variation:

2999152

HGVS (amino-acid)	Matching Registered Transcripts
NP_000343.2:p.Ala1369Thr	CA5902584 NM_000352.6:c.4105G>A