Canonical Allele Identifier: PA658800936
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543530
ClinVar RCV Id: RCV000654322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Gly52Ser
CA342629350
NM_000748.3:c.154G>A