Allele Registry

Canonical Allele Identifier: PA2499305844

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001350644

ClinVar Variation:

1046129

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg452Cys	CA3162839 NM_207352.4:c.1354C>T