Canonical Allele Identifier: PA2825047515
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 631776
ClinVar RCV Id: RCV000778502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Pro493_Ter494insGlnLeuAlaProThrSerIleSerHisProSerProValGlyAsn
CA287178757
NM_000080.4:c.1480T>C