Canonical Allele Identifier: PA645448794
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 379641
ClinVar RCV Id: RCV000422827 RCV000525258 RCV003889884
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Arg908Gln
CA1580206
NM_015662.3:c.2723G>A