Canonical Allele Identifier: PA645466800
Gene: IFT27 HGNC NCBI

Linked Data

ClinVar Variation Id: 377288
ClinVar RCV Id: RCV000443592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171172.1:p.Arg139Trp
CA10212351
NM_001177701.3:c.415C>T