Canonical Allele Identifier: PA2580102791
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2159155
ClinVar RCV Id: RCV003072667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Arg481Gly
CA397297346
NM_000080.4:c.1441C>G