Canonical Allele Identifier: PA2826619322
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 4638
ClinVar RCV Id: RCV000004901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267470.1:p.Trp7Cys
CA340279
NM_001280541.2:c.21G>C
CA354469060
NM_001280541.2:c.21G>T