Canonical Allele Identifier: PA2825799708
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1402408
ClinVar RCV Id: RCV001906426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Ala402Val
CA356826619
NM_001142564.2:c.1205C>T