Canonical Allele Identifier: PA2573162805
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1488514
ClinVar RCV Id: RCV002388996 RCV002592580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.His462Arg
CA345436290
NM_000143.4:c.1385A>G