Canonical Allele Identifier: PA2573261199
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431973
ClinVar RCV Id: RCV001941031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Met1411Thr
CA276668314
NM_014714.4:c.4232T>C