Canonical Allele Identifier: PA1139731586
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 957102
ClinVar RCV Id: RCV001230020 RCV001833988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061971.3:p.Lys147Asn
CA4800400
NM_019098.5:c.441G>T
CA371450137
NM_019098.5:c.441G>C