Canonical Allele Identifier: PA2825799802
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063017
ClinVar RCV Id: RCV001372809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Asp507His
CA356825389
NM_001142564.2:c.1519G>C