Canonical Allele Identifier: PA1139732236
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 939180
ClinVar RCV Id: RCV001208531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Ala762Val
CA4799757
NM_019098.5:c.2285C>T