Canonical Allele Identifier: PA2741813191
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2681942
ClinVar RCV Id: RCV003477234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala332Val
CA345438259
NM_000143.4:c.995C>T