Canonical Allele Identifier: PA2573213729
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1416835
ClinVar RCV Id: RCV001947995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Gly603Val
CA356823644
NM_001379270.1:c.1808G>T