Canonical Allele Identifier: PA1139679436
Gene: CHRNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 850367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000738.2:p.Val319Ala
CA397798178
NM_000747.3:c.956T>C