Canonical Allele Identifier: PA645440363
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410309
ClinVar RCV Id: RCV000465543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Ala135Val
CA16609870
NM_000748.3:c.404C>T