Canonical Allele Identifier: PA220383
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 29705
ClinVar RCV Id: RCV000022554 RCV000078149 RCV000492836 RCV003335052 RCV003483435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro174Arg
CA220381
NM_000143.4:c.521C>G