Canonical Allele Identifier: PA645465474
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 318200
ClinVar RCV Id: RCV000281495 RCV003165857 RCV002487403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Ser289Arg
CA7814525
NM_014714.4:c.867C>G
CA394217584
NM_014714.4:c.867C>A
CA394217594
NM_014714.4:c.865A>C