Canonical Allele Identifier: PA2580129435
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767064
ClinVar RCV Id: RCV002374050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val316Met
CA1130798
NM_000748.3:c.946G>A