Allele Registry

Canonical Allele Identifier: PA916030950

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000502822

ClinVar Variation:

434052

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338224.1:p.Gly1506Val	CA379783463 NM_001351295.2:c.4517G>T