Allele Registry

Canonical Allele Identifier: PA2827606175

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029262

RCV001818180

ClinVar Variation:

35615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Arg1378Leu	CA213457 NM_001351297.2:c.4133G>T