Allele Registry

Canonical Allele Identifier: PA2825056628

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV003468076

ClinVar Variation:

2675346

HGVS (amino-acid)	Matching Registered Transcripts
NP_000128.1:p.Glu364Gln	CA393621922 NM_000137.4:c.1090G>C