Canonical Allele Identifier: PA110442
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17496
ClinVar RCV Id: RCV000019048 RCV001091721 RCV001216785 RCV003493411 RCV004018644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val287Met
CA341464
NM_000748.3:c.859G>A