Allele Registry

Canonical Allele Identifier: PA891863413

Gene: ABCC2 HGNC NCBI

ClinVar RCV:

RCV000391369

ClinVar Variation:

289529

HGVS (amino-acid)	Matching Registered Transcripts
NP_000383.2:p.Trp709Arg	CA5643407 NM_000392.5:c.2125T>C CA378116437 NM_000392.5:c.2125T>A