Allele Registry

Canonical Allele Identifier: PA2827606000

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000626670

RCV001196917

RCV001249021

RCV001725116

RCV002243661

RCV002243662

RCV003234919

RCV004018675

ClinVar Variation:

35609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Val1172Met	CA213445 NM_001351297.2:c.3514G>A