Canonical Allele Identifier: PA645465517
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 317996
ClinVar RCV Id: RCV000389559 RCV003335305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Pro1263Leu
CA7813038
NM_014714.4:c.3788C>T