Canonical Allele Identifier: PA2826709254
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320070
ClinVar RCV Id: RCV000272670 RCV000755934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Asp945Glu
CA8082799
NM_001286130.2:c.2835C>A
CA396055902
NM_001286130.2:c.2835C>G