Allele Registry

Canonical Allele Identifier: PA2826156617

Gene: IFT80 HGNC NCBI

ClinVar RCV:

RCV000001046

RCV002512630

ClinVar Variation:

991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177170.1:p.Ala564Pro	CA114705 NM_001190241.2:c.1690G>C