Canonical Allele Identifier: PA2573173188
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379231
ClinVar RCV Id: RCV001883664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val136Met
CA1130725
NM_000748.3:c.406G>A