Canonical Allele Identifier: PA2580129389
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718971
ClinVar RCV Id: RCV002296736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Lys156Glu
CA342630086
NM_000748.3:c.466A>G