Canonical Allele Identifier: PA2829903398
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 4636
ClinVar RCV Id: RCV000004899
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060732.2:p.Ser263Phe
CA340276
NM_018262.4:c.788C>T