Canonical Allele Identifier: PA916010693
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 283739
ClinVar RCV Id: RCV000294633 RCV000794465 RCV002278283 RCV003278736
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267475.1:p.Phe954Ile
CA2606945
NM_001280546.2:c.2860T>A