Canonical Allele Identifier: PA2741944932
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630040
ClinVar RCV Id: RCV003391321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Glu1453Asp
CA394222235
NM_014714.4:c.4359G>T
CA394222236
NM_014714.4:c.4359G>C