Canonical Allele Identifier: PA098937
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 97024
ClinVar RCV Id: RCV000083270 RCV000201713 RCV003225027 RCV002483158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Arg1544Cys
CA149724
NM_015662.3:c.4630C>T