Allele Registry

Canonical Allele Identifier: PA213443

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV001823102

RCV002266905

RCV002266906

RCV003137542

ClinVar Variation:

35606

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Tyr539Cys	CA213441 NM_001287174.3:c.1616A>G