Canonical Allele Identifier: PA2573261197
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1489972
ClinVar RCV Id: RCV001978451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Pro1407Leu
CA394222514
NM_014714.4:c.4220C>T