Allele Registry

Canonical Allele Identifier: PA111258

Gene: CYP4V2 HGNC NCBI

ClinVar Allele:

47855

ClinVar RCV:

RCV000032526

ClinVar Variation:

39249

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ser341Pro	CA343705 NM_207352.4:c.1021T>C