Canonical Allele Identifier: PA658680225
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 485565
ClinVar RCV Id: RCV000571616 RCV000635311 RCV002528980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Arg74Ser
CA1478746
NM_000143.4:c.222A>T
CA345441782
NM_000143.4:c.222A>C