Canonical Allele Identifier: PA2573173203
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369115
ClinVar RCV Id: RCV001874581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Ser175Trp
CA30834161
NM_000748.3:c.524C>G