Allele Registry

Canonical Allele Identifier: PA111203

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032536

RCV000352220

RCV001074796

RCV001092654

ClinVar Variation:

39259

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Glu79Asp	CA343723 NM_207352.4:c.237G>T CA358946843 NM_207352.4:c.237G>C