Canonical Allele Identifier: PA645460472
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_443711.2:p.Phe1214Ile
CA2606945
NM_052985.4:c.3640T>A