Allele Registry

Canonical Allele Identifier: PA2499234429

Gene: CYP4F3 HGNC NCBI

ClinVar RCV:

RCV001531452

ClinVar Variation:

1176068

HGVS (amino-acid)	Matching Registered Transcripts
NP_000887.2:p.Thr83Ile	CA404553997 NM_000896.3:c.248C>T