Allele Registry

Canonical Allele Identifier: PA2828818326

Gene: CNGA1 HGNC NCBI

ClinVar RCV:

RCV000132618

ClinVar Variation:

143097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001366199.1:p.Asp326Gly	CA270044 NM_001379270.1:c.977A>G