Canonical Allele Identifier: PA658666885
Gene: CHRNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476148
ClinVar RCV Id: RCV000540432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000738.2:p.Arg335Cys
CA8347932
NM_000747.3:c.1003C>T