Canonical Allele Identifier: PA645382719
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 429166
ClinVar RCV Id: RCV000494364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ser186Cys
CA345439509
NM_000143.4:c.556A>T