Allele Registry

Canonical Allele Identifier: PA645461694

Gene: CYP2U1 HGNC NCBI

ClinVar RCV:

RCV000498760

ClinVar Variation:

433182

HGVS (amino-acid)	Matching Registered Transcripts
NP_898898.1:p.Pro151Leu	CA357833324 NM_183075.3:c.452C>T