Canonical Allele Identifier: PA313664
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205073
ClinVar RCV Id: RCV000186993 RCV001852445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Thr304Ala
CA313663
NM_000748.3:c.910A>G