Canonical Allele Identifier: PA2499229024
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1037512
ClinVar RCV Id: RCV002456480 RCV002546908
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly370Arg
CA345437868
NM_000143.4:c.1108G>C