Canonical Allele Identifier: PA658669571
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 451342
ClinVar RCV Id: RCV000523121 RCV001089402 RCV002467857 RCV004553148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Pro1025Ala
CA1580090
NM_015662.3:c.3073C>G