Canonical Allele Identifier: PA313650
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205066
ClinVar RCV Id: RCV000186986 RCV000416529 RCV001262983 RCV001213692 RCV002513986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Lys110Thr
CA313649
NM_000748.3:c.329A>C