Canonical Allele Identifier: PA2580363023
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1903279
ClinVar RCV Id: RCV002583580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Ser433Ala
CA394214552
NM_014714.4:c.1297T>G