Allele Registry

Canonical Allele Identifier: PA343711

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032529

RCV001852654

ClinVar Variation:

39252

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Pro396Leu	CA343710 NM_207352.4:c.1187C>T