Canonical Allele Identifier: PA112107
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 429176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Lys230Arg
CA1478630
NM_000143.4:c.689A>G