Canonical Allele Identifier: PA2826709287
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166891
ClinVar RCV Id: RCV000153040 RCV000504912 RCV001073599 RCV001331891 RCV001257781 RCV003907442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Asn980Ile
CA233760
NM_001286130.2:c.2939A>T