Allele Registry

Canonical Allele Identifier: PA2828508858

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV000012641

ClinVar Variation:

11866

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361306.1:p.Ala134Asp	CA256100 NM_001374377.1:c.401C>A