Canonical Allele Identifier: PA645382811
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 405911
ClinVar RCV Id: RCV000472774 RCV001025411 RCV001098958 RCV002523294 RCV003320643
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asp219Asn
CA1478641
NM_000143.4:c.655G>A