Canonical Allele Identifier: PA152419
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 128768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Gly18Val
CA152418
NM_000080.4:c.53G>T