Allele Registry

Canonical Allele Identifier: PA343725

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032537

RCV001377212

ClinVar Variation:

39260

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg85Cys	CA343724 NM_207352.4:c.253C>T