Canonical Allele Identifier: PA2826128145
Gene: IFT27 HGNC NCBI
ClinVar RCV:
RCV003023828
ClinVar Variation:
2110976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171172.1:p.Thr92Ile
CA10212418
NM_001177701.3:c.275C>T