Canonical Allele Identifier: PA2829903369
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_060732.2:p.Arg218Trp
CA2606009
NM_018262.4:c.652C>T