Canonical Allele Identifier: PA2580233707
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2177624
ClinVar RCV Id: RCV002585634
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361309.1:p.Asp27His
CA274011166
NM_001374380.1:c.79G>C