Canonical Allele Identifier: PA093073
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 13215
ClinVar RCV Id: RCV000014102 RCV000277104 RCV001092437 RCV003415696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Asp98Gly
CA122963
NM_000055.4:c.293A>G