Allele Registry

Canonical Allele Identifier: PA106816

Gene: CYP2U1 HGNC NCBI

ClinVar RCV:

RCV000032697

ClinVar Variation:

39501

HGVS (amino-acid)	Matching Registered Transcripts
NP_898898.1:p.Glu380Gly	CA130342 NM_183075.3:c.1139A>G