Canonical Allele Identifier: PA1139689388
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 949973
ClinVar RCV Id: RCV001221576 RCV001828766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Ile491Val
CA8313806
NM_000080.4:c.1471A>G