Canonical Allele Identifier: PA2573161051
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1416009
ClinVar RCV Id: RCV001921135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Asn480Ser
CA397297356
NM_000080.4:c.1439A>G