Canonical Allele Identifier: PA2580106965
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1755628
ClinVar RCV Id: RCV002369596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gln227His
CA345439251
NM_000143.4:c.681G>T
CA345439252
NM_000143.4:c.681G>C