Canonical Allele Identifier: PA199776
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 191369
ClinVar RCV Id: RCV000171551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Leu257Pro
CA199775
NM_015662.3:c.770T>C