Canonical Allele Identifier: PA2825799736
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 999735
ClinVar RCV Id: RCV001295771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Leu437Val
CA2911099
NM_001142564.2:c.1309C>G