Allele Registry

Canonical Allele Identifier: PA2826733974

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV003851783

ClinVar Variation:

2999152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Ala1370Thr	CA5902584 NM_001287174.3:c.4108G>A