Canonical Allele Identifier: PA1139731609
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 908889
ClinVar RCV Id: RCV001159642 RCV001159643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Pro158Leu
CA371450065
NM_019098.5:c.473C>T