Canonical Allele Identifier: PA2573162649
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1405050
ClinVar RCV Id: RCV002557578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr190Ile
CA345439481
NM_000143.4:c.569C>T