Canonical Allele Identifier: PA2826708964
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 195667
ClinVar RCV Id: RCV000291964 RCV000724483 RCV001074215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Arg731Cys
CA242185
NM_001286130.2:c.2191C>T