Canonical Allele Identifier: PA913198528
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 598611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Leu282Phe
CA342630954
NM_000748.3:c.844C>T