Canonical Allele Identifier: PA915961974
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 657553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Arg341Trp
CA397300799
NM_000080.4:c.1021C>T