Allele Registry

Canonical Allele Identifier: PA2825148798

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV001956958

ClinVar Variation:

1464709

HGVS (amino-acid)	Matching Registered Transcripts
NP_000343.2:p.Arg1420Ser	CA379786677 NM_000352.6:c.4258C>A