Canonical Allele Identifier: PA2499227878
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1157189
ClinVar RCV Id: RCV001500153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Ala488Thr
CA8313811
NM_000080.4:c.1462G>A