Canonical Allele Identifier: PA2580363290
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 2081690
ClinVar RCV Id: RCV002995538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Met1411Leu
CA394222493
NM_014714.4:c.4231A>T
CA394222495
NM_014714.4:c.4231A>C