Canonical Allele Identifier: PA658831163
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 547039
ClinVar RCV Id: RCV000659108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Asn68Ser
CA371456657
NM_019098.5:c.203A>G