Canonical Allele Identifier: PA2573261208
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436459
ClinVar RCV Id: RCV001987380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Met1444Val
CA7812783
NM_014714.4:c.4330A>G