Canonical Allele Identifier: PA2825547748
Gene: IFT43 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525543
ClinVar RCV Id: RCV002050380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096034.1:p.Leu4Met
CA390472805
NM_001102564.3:c.10T>A