Canonical Allele Identifier: PA095623
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 97054
ClinVar RCV Id: RCV000083298 RCV001075445 RCV001268554 RCV001542691 RCV003398688 RCV000626462 RCV002509205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Gly522Glu
CA149748
NM_014714.4:c.1565G>A