Allele Registry

Canonical Allele Identifier: PA2742038058

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV003548255

ClinVar Variation:

2713062

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg390Pro	CA358950220 NM_207352.4:c.1169G>C