Allele Registry

Canonical Allele Identifier: PA110927

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV000012647

ClinVar Variation:

11872

HGVS (amino-acid)	Matching Registered Transcripts
NP_000128.1:p.Arg381Gly	CA256105 NM_000137.4:c.1141A>G