Canonical Allele Identifier: PA1139678928
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 956825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly302Asp
CA345438434
NM_000143.4:c.905G>A