Canonical Allele Identifier: PA2741823432
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2758489
ClinVar RCV Id: RCV003583887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val321Leu
CA342631195
NM_000748.3:c.961G>T
CA342631196
NM_000748.3:c.961G>C