Canonical Allele Identifier: PA913191382
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 620130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Tyr478Ter
CA2576135543
NM_000080.4:c.1433dup