Canonical Allele Identifier: PA2573213724
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349273
ClinVar RCV Id: RCV002035172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Ser544Gly
CA356824805
NM_001379270.1:c.1630A>G