Canonical Allele Identifier: PA2825799711
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369499
ClinVar RCV Id: RCV001870665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Ile410Thr
CA356826491
NM_001142564.2:c.1229T>C