Allele Registry

Canonical Allele Identifier: PA111226

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032552

RCV000490060

RCV001074450

ClinVar Variation:

39275

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.His331Pro	CA343747 NM_207352.4:c.992A>C