Allele Registry

Canonical Allele Identifier: PA110432

Gene: CHRNB2 HGNC NCBI

ClinVar RCV:

RCV000019047

RCV002286498

RCV003097704

ClinVar Variation:

17495

1707538

HGVS (amino-acid)	Matching Registered Transcripts
NP_000739.1:p.Val287Leu	CA341463 NM_000748.3:c.859G>C CA343929 NM_000748.3:c.859G>T