Canonical Allele Identifier: PA2829904169
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_060732.2:p.Phe1104Ile
CA2606945
NM_018262.4:c.3310T>A