Canonical Allele Identifier: PA645440334
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418612
ClinVar RCV Id: RCV000486991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Tyr132His
CA16616984
NM_000748.3:c.394T>C