Canonical Allele Identifier: PA313652
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205067
ClinVar RCV Id: RCV000186987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Ile183Met
CA313651
NM_000748.3:c.549C>G