Canonical Allele Identifier: PA2580106925
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1707787
ClinVar RCV Id: RCV002286948 RCV002337432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly167Cys
CA345439965
NM_000143.4:c.499G>T