Allele Registry

Canonical Allele Identifier: PA3057471942

Gene: IFT172 HGNC NCBI

ClinVar RCV:

RCV005020950

ClinVar Variation:

3586371

HGVS (amino-acid)	Matching Registered Transcripts
NP_056477.1:p.Arg264Leu	CA44515401 NM_015662.3:c.791G>T