Canonical Allele Identifier: PA2499229049
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1061208
ClinVar RCV Id: RCV001370748 RCV001762647 RCV002420831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr68Cys
CA345441840
NM_000143.4:c.203A>G