Canonical Allele Identifier: PA658801124
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 529802
ClinVar RCV Id: RCV000635286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Cys377Tyr
CA345437584
NM_000143.4:c.1130G>A