Canonical Allele Identifier: PA1139696688
Gene: CNGA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 971798
ClinVar RCV Id: RCV001247667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289.1:p.His242Asp
CA1793882
NM_001298.3:c.724C>G