Canonical Allele Identifier: PA2828818377
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716368
ClinVar RCV Id: RCV002304667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Gly506Arg
CA356825396
NM_001379270.1:c.1516G>C
CA356825398
NM_001379270.1:c.1516G>A