Canonical Allele Identifier: PA2573260675
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406373
ClinVar RCV Id: RCV001915789 RCV002478343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Thr434Met
CA7814377
NM_014714.4:c.1301C>T