Canonical Allele Identifier: PA2828818395
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 812273
ClinVar RCV Id: RCV001002952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Phe540Cys
CA356824868
NM_001379270.1:c.1619T>G