Canonical Allele Identifier: PA2741809120
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 2603951
ClinVar RCV Id: RCV003350622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Cys9Gly
CA2692576
NM_000055.4:c.25T>G