Allele Registry

Canonical Allele Identifier: PA2499305827

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001349219

ClinVar Variation:

1044899

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ile77Phe	CA358946827 NM_207352.4:c.229A>T