Canonical Allele Identifier: PA1139679744
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954350
ClinVar RCV Id: RCV001226794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val313Ile
CA1130797
NM_000748.3:c.937G>A