Canonical Allele Identifier: PA2580232269
Gene: IFT27 HGNC NCBI

Linked Data

ClinVar Variation Id: 2110976
ClinVar RCV Id: RCV003023828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349932.1:p.Thr92Ile
CA10212418
NM_001363003.2:c.275C>T