Allele Registry

Canonical Allele Identifier: PA2827605077

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000502822

ClinVar Variation:

434052

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338225.1:p.Gly1484Val	CA379783463 NM_001351296.2:c.4451G>T