Canonical Allele Identifier: PA645465528
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 317984
ClinVar RCV Id: RCV000334851 RCV002494994 RCV002520984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Asp1461Asn
CA7812764
NM_014714.4:c.4381G>A