Canonical Allele Identifier: PA1139689193
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 962329
ClinVar RCV Id: RCV001236168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Leu342Pro
CA397300789
NM_000080.4:c.1025T>C