Canonical Allele Identifier: PA104511
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 5227
ClinVar RCV Id: RCV000005538 RCV000378015 RCV000497748 RCV000881356 RCV001276134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Tyr469Asp
CA340372
NM_019098.5:c.1405T>G