Canonical Allele Identifier: PA2826156808
Gene: IFT80 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040446
ClinVar RCV Id: RCV001344094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177171.1:p.Lys367Asn
CA2685135
NM_001190242.2:c.1101G>T
CA355191927
NM_001190242.2:c.1101G>C