Canonical Allele Identifier: PA159739
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 134414
ClinVar RCV Id: RCV000121089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ser24Trp
CA159737
NM_000143.4:c.71C>G