Canonical Allele Identifier: PA2580107032
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1767478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala320Thr
CA1478566
NM_000143.4:c.958G>A