Canonical Allele Identifier: PA2580129385
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2101033
ClinVar RCV Id: RCV003033646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Asn134Ser
CA342629944
NM_000748.3:c.401A>G