Allele Registry

Canonical Allele Identifier: PA2827606227

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV001956958

ClinVar Variation:

1464709

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Arg1419Ser	CA379786677 NM_001351297.2:c.4255C>A