Canonical Allele Identifier: PA2580102529
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1896707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Pro101Ala
CA397307047
NM_000080.4:c.301C>G