Canonical Allele Identifier: PA2830133041
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 343235
ClinVar RCV Id: RCV000272301
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443716.1:p.Arg166Trp
CA2606009
NM_052990.3:c.496C>T