Canonical Allele Identifier: PA072579
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 221925
ClinVar RCV Id: RCV000207410 RCV001853288 RCV003888642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Arg1294Cys
CA072574
NM_015662.3:c.3880C>T