Canonical Allele Identifier: PA2741809638
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2909841
ClinVar RCV Id: RCV003642196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Trp106Arg
CA397306978
NM_000080.4:c.316T>C
CA397306981
NM_000080.4:c.316T>A