Allele Registry

Canonical Allele Identifier: PA2827605526

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029251

RCV002052023

ClinVar Variation:

35605

1526003

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Phe535Leu	CA213438 NM_001351297.2:c.1603T>C CA379766367 NM_001351297.2:c.1605T>G CA379766368 NM_001351297.2:c.1605T>A