Canonical Allele Identifier: PA2499279087
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1004201
ClinVar RCV Id: RCV001300874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Met444Val
CA7814365
NM_014714.4:c.1330A>G