Allele Registry

Canonical Allele Identifier: PA2827605067

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000503504

RCV000710389

RCV000763232

RCV001848864

RCV003330733

RCV003470623

RCV004526403

ClinVar Variation:

434045

3233553

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338225.1:p.Gly1478Arg	CA218406864 NM_001351296.2:c.4432G>A CA379783645 NM_001351296.2:c.4432G>C