Canonical Allele Identifier: PA645465496
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 372905
ClinVar RCV Id: RCV000413732 RCV001042480 RCV001328310 RCV002298581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Pro726Ala
CA16042927
NM_014714.4:c.2176C>G