Canonical Allele Identifier: PA2580107051
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1803287
ClinVar RCV Id: RCV002466957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Glu355Val
CA345438082
NM_000143.4:c.1064A>T