Canonical Allele Identifier: PA320479
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 214380
ClinVar RCV Id: RCV002515397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly326Arg
CA320477
NM_000143.4:c.976G>A
CA345438299
NM_000143.4:c.976G>C