Allele Registry

Canonical Allele Identifier: PA2828083325

Gene: CFAP418 HGNC NCBI

ClinVar RCV:

RCV000024193

RCV000477682

RCV001002908

RCV001257837

RCV002228055

ClinVar Variation:

31194

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350189.1:p.Arg145Trp	CA260013 NM_001363260.1:c.433C>T