Canonical Allele Identifier: PA2573162679
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1435759
ClinVar RCV Id: RCV002562750 RCV004042926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Val240Leu
CA345439182
NM_000143.4:c.718G>C