Canonical Allele Identifier: PA2825799705
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2302518
ClinVar RCV Id: RCV002855581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Asn398His
CA2911115
NM_001142564.2:c.1192A>C