Canonical Allele Identifier: PA1139745069
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 901407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Ile413Val
CA2911108
NM_001379270.1:c.1237A>G