Allele Registry

Canonical Allele Identifier: PA2580570942

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV003019046

ClinVar Variation:

2097909

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg221Ser	CA358947818 NM_207352.4:c.661C>A