Canonical Allele Identifier: PA1139745085
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 934602
ClinVar RCV Id: RCV001203024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366199.1:p.Met590Thr
CA2911016
NM_001379270.1:c.1769T>C