Canonical Allele Identifier: PA2499229021
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1018142
ClinVar RCV Id: RCV002543724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly352Asp
CA345438118
NM_000143.4:c.1055G>A