Canonical Allele Identifier: PA2741972856
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2846435
ClinVar RCV Id: RCV003687891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Ser156Ala
CA371450079
NM_019098.5:c.466T>G