Canonical Allele Identifier: PA2741813183
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2561172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met328Leu
CA1478564
NM_000143.4:c.982A>C
CA345438288
NM_000143.4:c.982A>T