Allele Registry

Canonical Allele Identifier: PA645397429

Gene: IFT80 HGNC NCBI

ClinVar RCV:

RCV000336393

RCV001001024

RCV004021897

ClinVar Variation:

343967

HGVS (amino-acid)	Matching Registered Transcripts
NP_065851.1:p.Asn560Asp	CA2685070 NM_020800.3:c.1678A>G