Canonical Allele Identifier: PA2580363022
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 2132756
ClinVar RCV Id: RCV003063868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Phe431Leu
CA394214564
NM_014714.4:c.1293C>G
CA394214566
NM_014714.4:c.1293C>A
CA394214576
NM_014714.4:c.1291T>C