Canonical Allele Identifier: PA658665899
Gene: CHRNE HGNC NCBI

Linked Data

ClinVar Variation Id: 465849
ClinVar RCV Id: RCV000547397 RCV002263775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000071.1:p.Pro340Leu
CA8314074
NM_000080.4:c.1019C>T