Canonical Allele Identifier: PA2580129381
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444605
ClinVar RCV Id: RCV003154381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Ala123Val
CA342629872
NM_000748.3:c.368C>T