Canonical Allele Identifier: PA1139745092
Gene: CNGA1 HGNC NCBI
ClinVar RCV:
RCV001232063
ClinVar Variation:
958826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Arg639Gln
CA2910996
NM_001379270.1:c.1916G>A