Canonical Allele Identifier: PA915960653
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 823349
ClinVar RCV Id: RCV001019524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala320Val
CA40327914
NM_000143.4:c.959C>T