Canonical Allele Identifier: PA645382714
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 432129
ClinVar RCV Id: RCV000498190 RCV001196074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.His176Arg
CA345439904
NM_000143.4:c.527A>G