Canonical Allele Identifier: PA658674118
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 446311
ClinVar RCV Id: RCV000515594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Leu1399Pro
CA7812832
NM_014714.4:c.4196T>C