Allele Registry

Canonical Allele Identifier: PA343746

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032551

RCV001362372

ClinVar Variation:

39274

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Thr325Ile	CA343745 NM_207352.4:c.974C>T