Allele Registry

Canonical Allele Identifier: PA1139730192

Gene: ABCC8 HGNC NCBI

ClinVar Allele:

978945

ClinVar RCV:

RCV001279206

RCV002254207

RCV002254208

ClinVar Variation:

991064

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Cys170Gly	CA379779996 NM_001351297.2:c.508T>G