Canonical Allele Identifier: PA2826709295
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8897
ClinVar RCV Id: RCV000009448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Gly987Val
CA254576
NM_001286130.2:c.2960G>T