Allele Registry

Canonical Allele Identifier: PA2825148559

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV002010847

ClinVar Variation:

1501932

HGVS (amino-acid)	Matching Registered Transcripts
NP_000343.2:p.Ala1184Val	CA379797331 NM_000352.6:c.3551C>T