Canonical Allele Identifier: PA645465516
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 317997
ClinVar RCV Id: RCV000278956 RCV003165856 RCV002487400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Arg1260Gln
CA7813040
NM_014714.4:c.3779G>A