Canonical Allele Identifier: PA2829663387
Gene: IFT27 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462480
ClinVar RCV Id: RCV001954269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006851.1:p.Arg138Gly
CA411381564
NM_006860.5:c.412C>G