Allele Registry

Canonical Allele Identifier: PA351255

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV001041757

RCV001272485

ClinVar Variation:

242507

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Tyr398Cys	CA351254 NM_019098.5:c.1193A>G