Canonical Allele Identifier: PA112055
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 92455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asn107Thr
CA257456
NM_000143.4:c.320A>C