Canonical Allele Identifier: PA2580106905
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1738561
ClinVar RCV Id: RCV002327772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Val140Ile
CA1478681
NM_000143.4:c.418G>A