Canonical Allele Identifier: PA2826619349
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 282987
ClinVar RCV Id: RCV000400100 RCV002480008
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267470.1:p.Val77Ile
CA2605752
NM_001280541.2:c.229G>A