Allele Registry

Canonical Allele Identifier: PA645438635

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000502822

ClinVar Variation:

434052

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Gly1485Val	CA379783463 NM_001287174.3:c.4454G>T