Canonical Allele Identifier: PA2826367268
Gene: IFT43 HGNC NCBI

Linked Data

ClinVar Variation Id: 314467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242924.1:p.Ala31Val
CA7280635
NM_001255995.3:c.92C>T