Canonical Allele Identifier: PA658809369
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 523181
ClinVar RCV Id: RCV000626464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Pro726Leu
CA394203209
NM_014714.4:c.2177C>T