Canonical Allele Identifier: PA2826128177
Gene: IFT27 HGNC NCBI
ClinVar RCV:
RCV001063722
ClinVar Variation:
857948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171172.1:p.Val154Met
CA10212339
NM_001177701.3:c.460G>A