Canonical Allele Identifier: PA891845509
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 565991
ClinVar RCV Id: RCV001012881 RCV001731888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly58Ser
CA345441941
NM_000143.4:c.172G>A