Canonical Allele Identifier: PA658831189
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 554970
ClinVar RCV Id: RCV000670701 RCV001245682 RCV001830448
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Gly795Arg
CA4799736
NM_019098.5:c.2383G>A
CA371446056
NM_019098.5:c.2383G>C