Canonical Allele Identifier: PA645465459
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 318216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Leu100Val
CA7814755
NM_014714.4:c.298C>G