Allele Registry

Canonical Allele Identifier: PA2827606010

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV002894028

ClinVar Variation:

2028930

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Arg1181Leu	CA5902785 NM_001351297.2:c.3542G>T