Canonical Allele Identifier: PA2573272328
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379435
ClinVar RCV Id: RCV001891986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Lys117Arg
CA371450327
NM_019098.5:c.350A>G