Canonical Allele Identifier: PA2826619512
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 343244
ClinVar RCV Id: RCV000288140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267470.1:p.His578Gln
CA2606281
NM_001280541.2:c.1734C>G
CA354477243
NM_001280541.2:c.1734C>A