Canonical Allele Identifier: PA095669
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 97053
ClinVar RCV Id: RCV000083297 RCV000626469 RCV000515922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Val292Met
CA149747
NM_014714.4:c.874G>A