Canonical Allele Identifier: PA2499228996
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1024082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met164Ile
CA345439980
NM_000143.4:c.492G>T
CA345439981
NM_000143.4:c.492G>C
CA345439982
NM_000143.4:c.492G>A