Allele Registry

Canonical Allele Identifier: PA2828508763

Gene: FAH HGNC NCBI

ClinVar RCV:

RCV000012640

ClinVar Variation:

11865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361306.1:p.Asn16Ile	CA256099 NM_001374377.1:c.47A>T