Allele Registry

Canonical Allele Identifier: PA645376673

Gene: CYP4V2 HGNC NCBI

ClinVar Variation Id: 348313

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Glu447Lys	CA3162835 NM_207352.4:c.1339G>A