Canonical Allele Identifier: PA2825056301
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1685807
ClinVar RCV Id: RCV002249974
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000128.1:p.Val21Phe
CA393615587
NM_000137.4:c.61G>T