Canonical Allele Identifier: PA285331
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 92458
ClinVar RCV Id: RCV000078152 RCV000445608 RCV000762893 RCV002371923 RCV003460742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.His318Tyr
CA285329
NM_000143.4:c.952C>T