Canonical Allele Identifier: PA109525
Gene: IFT27 HGNC NCBI
ClinVar Allele:
150146
ClinVar RCV:
RCV000128641
ClinVar Variation:
140462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171172.1:p.Cys100Tyr
CA163415
NM_001177701.3:c.299G>A