Allele Registry

Canonical Allele Identifier: PA2827604954

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029262

RCV001818180

ClinVar Variation:

35615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338225.1:p.Arg1379Leu	CA213457 NM_001351296.2:c.4136G>T