Canonical Allele Identifier: PA2826128169
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_001171172.1:p.Arg139Gly
CA411381564
NM_001177701.3:c.415C>G