Canonical Allele Identifier: PA2573162704
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1413368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Leu303Phe
CA345438428
NM_000143.4:c.909G>T
CA345438429
NM_000143.4:c.909G>C