Canonical Allele Identifier: PA2499279057
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052590
ClinVar RCV Id: RCV001360807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Asp1116Glu
CA394225357
NM_014714.4:c.3348C>G
CA394225358
NM_014714.4:c.3348C>A