Allele Registry

Canonical Allele Identifier: PA3057587362

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV005254202

ClinVar Variation:

3776220

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Leu258Pro	CA358948097 NM_207352.4:c.773T>C