Canonical Allele Identifier: PA165196
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 141355
ClinVar RCV Id: RCV000129845 RCV000153237 RCV000549060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Arg233Cys
CA165194
NM_000143.4:c.697C>T