Canonical Allele Identifier: PA2830133191
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 4635
ClinVar RCV Id: RCV000004898
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443716.1:p.Val391Gly
CA340274
NM_052990.3:c.1172T>G