Allele Registry

Canonical Allele Identifier: PA341692

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000020289

ClinVar Variation:

21168

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Asp209Glu	CA341691 NM_001287174.3:c.627C>A CA379779047 NM_001287174.3:c.627C>G