Canonical Allele Identifier: PA1139739586
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 956202
ClinVar RCV Id: RCV001228961 RCV002504304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Arg441His
CA7814369
NM_014714.4:c.1322G>A