Allele Registry

Canonical Allele Identifier: PA343739

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032547

RCV002513306

ClinVar Variation:

39270

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.His254Arg	CA343738 NM_207352.4:c.761A>G