Canonical Allele Identifier: PA645440333
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373511
ClinVar RCV Id: RCV000413172 RCV001220609 RCV002265750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Gly125Ser
CA16042306
NM_000748.3:c.373G>A