Allele Registry

Canonical Allele Identifier: PA2827604101

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000145007

ClinVar Variation:

157709

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338225.1:p.His292Pro	CA270980 NM_001351296.2:c.875A>C