Canonical Allele Identifier: PA645382879
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 237117
ClinVar RCV Id: RCV002518307
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr234Ile
CA10581783
NM_000143.4:c.701C>T