Canonical Allele Identifier: PA1139679653
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 870606
ClinVar RCV Id: RCV001090182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Tyr139Ser
CA342629971
NM_000748.3:c.416A>C