Canonical Allele Identifier: PA658669578
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 451341
ClinVar RCV Id: RCV000520966 RCV001239376 RCV003483653 RCV004553147 RCV002476063
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Val1556Met
CA1579519
NM_015662.3:c.4666G>A