Allele Registry

Canonical Allele Identifier: PA343928

Gene: CHRNB2 HGNC NCBI

ClinVar RCV:

RCV004819093

ClinVar Variation:

3391473

HGVS (amino-acid)	Matching Registered Transcripts
NP_000739.1:p.Val337Gly	CA343927 NM_000748.3:c.1010T>G