Canonical Allele Identifier: PA915960471
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 819805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr56Ser
CA345441960
NM_000143.4:c.167C>G
CA345441962
NM_000143.4:c.166A>T