Allele Registry

Canonical Allele Identifier: PA2827606013

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV002010847

ClinVar Variation:

1501932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Ala1183Val	CA379797331 NM_001351297.2:c.3548C>T