Canonical Allele Identifier: PA2826619948
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 4635
ClinVar RCV Id: RCV000004898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267474.1:p.Val352Gly
CA340274
NM_001280545.2:c.1055T>G