Canonical Allele Identifier: PA215565
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 41584
ClinVar RCV Id: RCV000034486 RCV000471678 RCV000568576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Leu303Ser
CA215563
NM_000143.4:c.908T>C