Canonical Allele Identifier: PA2741954905
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 2935458
ClinVar RCV Id: RCV003791112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Cys409Arg
CA346393926
NM_015662.3:c.1225T>C