Allele Registry

Canonical Allele Identifier: PA206065

Gene: ABCC8 HGNC NCBI

ClinVar Allele:

207846

ClinVar RCV:

RCV000192916

RCV001640282

RCV002051825

RCV002500586

RCV002517038

RCV003987437

ClinVar Variation:

210076

HGVS (amino-acid)	Matching Registered Transcripts
NP_000343.2:p.Arg1182Trp	CA206064 NM_000352.6:c.3544C>T