Canonical Allele Identifier: PA093338
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 13227
ClinVar RCV Id: RCV000014131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Tyr156Cys
CA122970
NM_000055.4:c.467A>G