Canonical Allele Identifier: PA1139740501
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 957159
ClinVar RCV Id: RCV001230090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Tyr1396Cys
CA394222580
NM_014714.4:c.4187A>G