Canonical Allele Identifier: PA2828508887
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1343304
ClinVar RCV Id: RCV001843906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361306.1:p.Ser169Phe
CA393619863
NM_001374377.1:c.506C>T