Allele Registry

Canonical Allele Identifier: PA2499305847

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001327200

ClinVar Variation:

1026716

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ile468Val	CA112135313 NM_207352.4:c.1402A>G