Canonical Allele Identifier: PA1139731570
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 909751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Asp129Glu
CA371450249
NM_019098.5:c.387T>G
CA371450250
NM_019098.5:c.387T>A