Canonical Allele Identifier: PA658801032
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 529803
ClinVar RCV Id: RCV002358784 RCV002529839 RCV003459516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr2Cys
CA345443111
NM_000143.4:c.5A>G