Canonical Allele Identifier: PA2825799765
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1999294
ClinVar RCV Id: RCV002797097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Lys472Asn
CA2911081
NM_001142564.2:c.1416G>T
CA2911082
NM_001142564.2:c.1416G>C