Canonical Allele Identifier: PA233761
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166891
ClinVar RCV Id: RCV000153040 RCV000504912 RCV001073599 RCV001331891 RCV001257781 RCV003907442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288.3:p.Asn986Ile
CA233760
NM_001297.5:c.2957A>T