Canonical Allele Identifier: PA200692
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193628
ClinVar RCV Id: RCV000173736 RCV000371837 RCV000755238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288.3:p.Thr212Ser
CA200691
NM_001297.5:c.634A>T
CA396077788
NM_001297.5:c.635C>G