Canonical Allele Identifier: PA645382513
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 265145
ClinVar RCV Id: RCV000254803 RCV001062945 RCV002429193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr72Pro
CA10588293
NM_000143.4:c.214A>C