Allele Registry

Canonical Allele Identifier: PA2826733559

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV002279120

ClinVar Variation:

1702802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Gly716Asp	CA379813706 NM_001287174.3:c.2147G>A