Canonical Allele Identifier: PA916010666
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 283378
ClinVar RCV Id: RCV000399070 RCV000945510 RCV001582907 RCV003278735 RCV003939973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267474.1:p.Ile56Thr
CA2605932
NM_001280545.2:c.167T>C