Canonical Allele Identifier: PA129902
Gene: FUZ HGNC NCBI

Linked Data

ClinVar Variation Id: 31934
ClinVar RCV Id: RCV000024613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079405.2:p.Pro39Ser
CA129901
NM_025129.5:c.115C>T