Canonical Allele Identifier: PA645440401
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421485
ClinVar RCV Id: RCV000484907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val313Ala
CA16616985
NM_000748.3:c.938T>C