Allele Registry

Canonical Allele Identifier: PA2828509033

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV000012644

RCV003321481

ClinVar Variation:

11869

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361306.1:p.Gly337Ser	CA341148 NM_001374377.1:c.1009G>A