Canonical Allele Identifier: PA2580434518
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1910819
ClinVar RCV Id: RCV002589395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Thr800Ile
CA371446021
NM_019098.5:c.2399C>T