Canonical Allele Identifier: PA645440571
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 421400
ClinVar RCV Id: RCV000487143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Ile473Met
CA16620462
NM_000080.4:c.1419C>G