Canonical Allele Identifier: PA343933
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41035
ClinVar RCV Id: RCV000430538 RCV001382226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val308Ala
CA343932
NM_000748.3:c.923T>C