Canonical Allele Identifier: PA645433238
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 363874
ClinVar RCV Id: RCV000327065 RCV000363049 RCV001346392 RCV001828364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Tyr387Cys
CA10631709
NM_019098.5:c.1160A>G