Canonical Allele Identifier: PA2830132628
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_443715.1:p.Gly572Val
CA236202
NM_052989.3:c.1715G>T