Canonical Allele Identifier: PA277671
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 191356
ClinVar RCV Id: RCV000201484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Gly1276Glu
CA277670
NM_014714.4:c.3827G>A