Canonical Allele Identifier: PA2826620255
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 4636
ClinVar RCV Id: RCV000004899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267475.1:p.Ser113Phe
CA340276
NM_001280546.2:c.338C>T