Canonical Allele Identifier: PA197227
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 187279
ClinVar RCV Id: RCV000166997 RCV000469505 RCV001101030 RCV003320130 RCV002516512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ile120Val
CA197225
NM_000143.4:c.358A>G