Canonical Allele Identifier: PA322590
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 214428
ClinVar RCV Id: RCV002399736 RCV002517215
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Glu53Lys
CA322588
NM_000143.4:c.157G>A