Canonical Allele Identifier: PA1139739633
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 961914
ClinVar RCV Id: RCV001235678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Asp443Asn
CA7814367
NM_014714.4:c.1327G>A