Allele Registry

Canonical Allele Identifier: PA2580570965

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV003054527

ClinVar Variation:

2119167

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Cys406Tyr	CA112134823 NM_207352.4:c.1217G>A