Allele Registry

Canonical Allele Identifier: PA213449

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029256

RCV002243663

RCV002243664

ClinVar Variation:

35610

HGVS (amino-acid)	Matching Registered Transcripts
NP_000343.2:p.Phe1181Cys	CA213448 NM_000352.6:c.3542T>G