Canonical Allele Identifier: PA2826619976
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 343244
ClinVar RCV Id: RCV000288140
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267474.1:p.His436Gln
CA2606281
NM_001280545.2:c.1308C>G
CA354477243
NM_001280545.2:c.1308C>A