Canonical Allele Identifier: PA2826620205
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 283739
ClinVar RCV Id: RCV000294633 RCV000794465 RCV002278283 RCV003278736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267474.1:p.Phe1013Ile
CA2606945
NM_001280545.2:c.3037T>A