Canonical Allele Identifier: PA2829903699
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_060732.2:p.His527Gln
CA2606281
NM_018262.4:c.1581C>G
CA354477243
NM_018262.4:c.1581C>A