Allele Registry

Canonical Allele Identifier: PA093798

Gene: CNGA3 HGNC NCBI

ClinVar RCV:

RCV000010084

RCV000169654

RCV001002972

RCV001074603

RCV001219847

RCV002512958

ClinVar Variation:

9476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289.1:p.Gly557Arg	CA199157 NM_001298.3:c.1669G>A CA347834040 NM_001298.3:c.1669G>C