Allele Registry

Canonical Allele Identifier: PA343722

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032535

ClinVar Variation:

39258

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Pro509Leu	CA343721 NM_207352.4:c.1526C>T