Canonical Allele Identifier: PA891855987
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 569750
ClinVar RCV Id: RCV000690456 RCV004025054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Gly298Ser
CA1130792
NM_000748.3:c.892G>A