Allele Registry

Canonical Allele Identifier: PA2825056288

Gene: FAH HGNC NCBI

ClinVar Variation Id: 2811930

ClinVar RCV Id: RCV003634653

ClinVar Variation Id: 3065539

ClinVar RCV Id: RCV003990616

HGVS (amino-acid)	Matching Registered Transcripts
NP_000128.1:p.Phe12Leu	CA393615478 NM_000137.4:c.34T>C CA393615483 NM_000137.4:c.36C>A CA393615485 NM_000137.4:c.36C>G