Canonical Allele Identifier: PA916043645
Gene: IFT27 HGNC NCBI
ClinVar RCV:
RCV000968422
ClinVar Variation:
786380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349932.1:p.Ala142Val
CA10212348
NM_001363003.2:c.425C>T