Canonical Allele Identifier: PA1139731652
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 991603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Gln163His
CA4800389
NM_019098.5:c.489A>T
CA371450033
NM_019098.5:c.489A>C