Canonical Allele Identifier: PA2580378029
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 2143608
ClinVar RCV Id: RCV003053126 RCV003250718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Arg296Gln
CA1580841
NM_015662.3:c.887G>A