Canonical Allele Identifier: PA2828508803
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 21054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361306.1:p.Gln64His
CA233966
NM_001374377.1:c.192G>T
CA393618043
NM_001374377.1:c.192G>C