Allele Registry

Canonical Allele Identifier: PA2580216007

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV002279120

ClinVar Variation:

1702802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338224.1:p.Gly738Asp	CA379813706 NM_001351295.2:c.2213G>A