Allele Registry

Canonical Allele Identifier: PA163416

Gene: IFT27 HGNC NCBI

ClinVar Allele:

150146

ClinVar RCV:

RCV000128641

ClinVar Variation:

140462

HGVS (amino-acid)	Matching Registered Transcripts
NP_006851.1:p.Cys99Tyr	CA163415 NM_006860.5:c.296G>A