Allele Registry

Canonical Allele Identifier: PA2826987738

Gene: IFT56 HGNC NCBI

ClinVar RCV:

RCV002895201

RCV003903799

ClinVar Variation:

2038770

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305262.1:p.Asp170Asn	CA4508280 NM_001318333.2:c.508G>A