Canonical Allele Identifier: PA2580233748
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1896364
ClinVar RCV Id: RCV002575145 RCV004064320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361309.1:p.Met177Val
CA393619904
NM_001374380.1:c.529A>G