Allele Registry

Canonical Allele Identifier: PA1139735926

Gene: IFT172 HGNC NCBI

ClinVar RCV:

RCV001044874

RCV001550209

RCV003890180

RCV004553578

ClinVar Variation:

842448

HGVS (amino-acid)	Matching Registered Transcripts
NP_056477.1:p.Arg1455Trp	CA1579633 NM_015662.3:c.4363C>T