Allele Registry

Canonical Allele Identifier: PA120111

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000009670

RCV000020286

RCV001851772

RCV002051781

ClinVar Variation:

9102

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Phe132Leu	CA120110 NM_001287174.3:c.394T>C CA379783873 NM_001287174.3:c.396C>G CA379783874 NM_001287174.3:c.396C>A