Allele Registry

Canonical Allele Identifier: PA916031009

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000020289

ClinVar Variation:

21168

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Asp209Glu	CA341691 NM_001351297.2:c.627C>A CA379779047 NM_001351297.2:c.627C>G