Canonical Allele Identifier: PA2826058457
Gene: IFT46 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162089.1:p.Asn290Ser
CA6305604
NM_001168618.2:c.869A>G