Canonical Allele Identifier: PA2499234108
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1042753
ClinVar RCV Id: RCV001346762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Gly298Val
CA342631051
NM_000748.3:c.893G>T