Canonical Allele Identifier: PA645440328
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420484
ClinVar RCV Id: RCV000482418 RCV001244619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Thr93Ser
CA1130691
NM_000748.3:c.277A>T
CA342629648
NM_000748.3:c.278C>G