Allele Registry

Canonical Allele Identifier: PA916074347

Gene: CYP4V2 HGNC NCBI

ClinVar Allele:

790462

ClinVar RCV:

RCV000987493

RCV001869345

ClinVar Variation:

802105

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg390Leu	CA358950221 NM_207352.4:c.1169G>T