Allele Registry

Canonical Allele Identifier: PA2741828424

Gene: CYP4F2 HGNC NCBI

ClinVar RCV:

RCV003979017

ClinVar Variation:

3056325

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073.3:p.Leu519Met	CA9273540 NM_001082.5:c.1555C>A