Canonical Allele Identifier: PA658801060
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 529825
ClinVar RCV Id: RCV002528877 RCV003352953 RCV003493684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr56Ala
CA345441963
NM_000143.4:c.166A>G