Allele Registry

Canonical Allele Identifier: PA2827075479

Gene: IFT56 HGNC NCBI

ClinVar RCV:

RCV002895201

RCV003903799

ClinVar Variation:

2038770

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308669.1:p.Asp310Asn	CA4508280 NM_001321740.2:c.928G>A