Canonical Allele Identifier: PA1139688967
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 858675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Asp79Tyr
CA397307377
NM_000080.4:c.235G>T