Allele Registry

Canonical Allele Identifier: PA2741870711

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV003468076

ClinVar Variation:

2675346

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361309.1:p.Glu364Gln	CA393621922 NM_001374380.1:c.1090G>C