Allele Registry

Canonical Allele Identifier: PA130792

Gene: CHRNE HGNC NCBI

ClinVar RCV:

RCV000033234

ClinVar Variation:

40227

HGVS (amino-acid)	Matching Registered Transcripts
NP_000071.1:p.Ser298del	CA130791 NM_000080.4:c.892_894del CA2695224236 NM_000080.4:c.893_895del