Canonical Allele Identifier: PA658680352
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 460378
ClinVar RCV Id: RCV000525718 RCV000573963 RCV001551931
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr270Cys
CA1478602
NM_000143.4:c.809A>G