Allele Registry

Canonical Allele Identifier: PA110947

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV000020128

ClinVar Variation:

21057

HGVS (amino-acid)	Matching Registered Transcripts
NP_000128.1:p.Asp233Val	CA341565 NM_000137.4:c.698A>T