Canonical Allele Identifier: PA2573261198
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349781
ClinVar RCV Id: RCV002039263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Met1411Arg
CA7812819
NM_014714.4:c.4232T>G