Canonical Allele Identifier: PA313640
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205061
ClinVar RCV Id: RCV000186981 RCV000531578 RCV001704976 RCV002314695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Thr26Met
CA313639
NM_000748.3:c.77C>T