Canonical Allele Identifier: PA1139745072
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 957113
ClinVar RCV Id: RCV001230033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Arg429Ser
CA356826159
NM_001379270.1:c.1287G>T
CA356826161
NM_001379270.1:c.1287G>C