Canonical Allele Identifier: PA2741813286
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2562372
ClinVar RCV Id: RCV003310432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met454Val
CA345436399
NM_000143.4:c.1360A>G