Canonical Allele Identifier: PA1139679739
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 840970
ClinVar RCV Id: RCV001043096 RCV001809964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Leu307Ile
CA30834668
NM_000748.3:c.919C>A