Canonical Allele Identifier: PA658680511
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 485577
ClinVar RCV Id: RCV000565062 RCV002528983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr491Cys
CA40371583
NM_000143.4:c.1472A>G