Canonical Allele Identifier: PA2825799709
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1921270
ClinVar RCV Id: RCV002608751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Ala408Pro
CA356826530
NM_001142564.2:c.1222G>C