Canonical Allele Identifier: PA321907
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 214390
ClinVar RCV Id: RCV000197441 RCV000456662 RCV001013787
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asp65Gly
CA321905
NM_000143.4:c.194A>G