Canonical Allele Identifier: PA110442
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17496

Amino-acid Alleles

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