Allele Registry

Canonical Allele Identifier: PA2827605117

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029269

ClinVar Variation:

35622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338225.1:p.Val1522Met	CA213467 NM_001351296.2:c.4564G>A