Canonical Allele Identifier: PA098950
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 97028
ClinVar RCV Id: RCV000083274 RCV001303423 RCV002490732 RCV003153361 RCV004549522 RCV003278664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Arg296Trp
CA149729
NM_015662.3:c.886C>T