Canonical Allele Identifier: PA2825799702
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044892
ClinVar RCV Id: RCV001349212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Ile392Val
CA2911117
NM_001142564.2:c.1174A>G