Canonical Allele Identifier: PA2825799713
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2093413
ClinVar RCV Id: RCV003018717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Ala412Thr
CA356826462
NM_001142564.2:c.1234G>A