Allele Registry

Canonical Allele Identifier: PA2573094935

Gene: CFAP298 HGNC NCBI

ClinVar Allele:

1053660

ClinVar RCV:

RCV001732152

ClinVar Variation:

1065354

HGVS (amino-acid)	Matching Registered Transcripts
NP_067077.1:p.Ala103Asp	CA410075173 NM_021254.3:c.308C>A