Canonical Allele Identifier: PA2826619341
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 343230
ClinVar RCV Id: RCV000348801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267470.1:p.Arg67Ser
CA2605742
NM_001280541.2:c.199C>A