Canonical Allele Identifier: PA2826620342
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 191184
ClinVar RCV Id: RCV000171370 RCV003989481
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267475.1:p.Gly363Val
CA236202
NM_001280546.2:c.1088G>T