Canonical Allele Identifier: PA1139679141
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 840816
ClinVar RCV Id: RCV002552513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Leu335Val
CA345438242
NM_000143.4:c.1003C>G