Canonical Allele Identifier: PA2825799939
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2186749
ClinVar RCV Id: RCV002606875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Met647Thr
CA2910987
NM_001142564.2:c.1940T>C