Canonical Allele Identifier: PA2580363208
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 2330689
ClinVar RCV Id: RCV002935049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Ala1127Thr
CA394225298
NM_014714.4:c.3379G>A