Allele Registry

Canonical Allele Identifier: PA658702680

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000585008

RCV004526709

ClinVar Variation:

493483

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Ser4Leu	CA4800550 NM_019098.5:c.11C>T