Canonical Allele Identifier: PA1139732256
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 958631
ClinVar RCV Id: RCV001231829 RCV001834009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Ala807Ser
CA371445979
NM_019098.5:c.2419G>T