Canonical Allele Identifier: PA112046
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 16236
ClinVar RCV Id: RCV000017623 RCV000196988 RCV000178717 RCV000493379 RCV003128387 RCV003330393 RCV004541007
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Arg233His
CA257459
NM_000143.4:c.698G>A