Canonical Allele Identifier: PA2825799897
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 934602
ClinVar RCV Id: RCV001203024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Met590Thr
CA2911016
NM_001142564.2:c.1769T>C