Allele Registry

Canonical Allele Identifier: PA2827604777

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000626670

RCV001196917

RCV001249021

RCV001725116

RCV002243661

RCV002243662

RCV003234919

RCV004018675

ClinVar Variation:

35609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338225.1:p.Val1173Met	CA213445 NM_001351296.2:c.3517G>A