Canonical Allele Identifier: PA658665916
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 465855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Ala381Val
CA8314003
NM_000080.4:c.1142C>T