Allele Registry

Canonical Allele Identifier: PA2573317503

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV002025961

ClinVar Variation:

1504134

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Leu258Phe	CA358948095 NM_207352.4:c.772C>T