Canonical Allele Identifier: PA112123
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 529812
ClinVar RCV Id: RCV001784209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Phe312Cys
CA345438376
NM_000143.4:c.935T>G