Canonical Allele Identifier: PA2499281828
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000537
ClinVar RCV Id: RCV001296682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Pro280Arg
CA346397185
NM_015662.3:c.839C>G