Allele Registry

Canonical Allele Identifier: PA2828508986

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV000012650

ClinVar Variation:

11875

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361306.1:p.Gln279Arg	CA256106 NM_001374377.1:c.836A>G