Allele Registry

Canonical Allele Identifier: PA2826733854

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV002010847

ClinVar Variation:

1501932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Ala1185Val	CA379797331 NM_001287174.3:c.3554C>T