Canonical Allele Identifier: PA2741870696
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2675349
ClinVar RCV Id: RCV003468078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361309.1:p.Gly343Glu
CA393621786
NM_001374380.1:c.1028G>A