Canonical Allele Identifier: PA1139741081
Gene: IFT27 HGNC NCBI

Linked Data

ClinVar Variation Id: 857948
ClinVar RCV Id: RCV001063722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349932.1:p.Val154Met
CA10212339
NM_001363003.2:c.460G>A