Canonical Allele Identifier: PA2573162716
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1511238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ser325Cys
CA345438306
NM_000143.4:c.973A>T