Canonical Allele Identifier: PA2825053564
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 143097
ClinVar RCV Id: RCV000132618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000078.3:p.Asp326Gly
CA270044
NM_000087.5:c.977A>G