Allele Registry

Canonical Allele Identifier: PA213459

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029262

RCV001818180

ClinVar Variation:

35615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Arg1380Leu	CA213457 NM_001287174.3:c.4139G>T