Allele Registry

Canonical Allele Identifier: PA213472

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000501531

RCV000984138

RCV001762057

RCV002243673

RCV002243674

RCV003234921

ClinVar Variation:

35623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Val1540Met	CA213470 NM_001287174.3:c.4618G>A