Canonical Allele Identifier: PA2573173212
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1461202
ClinVar RCV Id: RCV001965741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val191Leu
CA342630379
NM_000748.3:c.571G>T
CA342630380
NM_000748.3:c.571G>C