Allele Registry

Canonical Allele Identifier: PA110966

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV000012650

ClinVar Variation:

11875

HGVS (amino-acid)	Matching Registered Transcripts
NP_000128.1:p.Gln279Arg	CA256106 NM_000137.4:c.836A>G