Allele Registry

Canonical Allele Identifier: PA199776

Gene: IFT172 HGNC NCBI

ClinVar RCV:

RCV000171551

ClinVar Variation:

191369

HGVS (amino-acid)	Matching Registered Transcripts
NP_056477.1:p.Leu257Pro	CA199775 NM_015662.3:c.770T>C