Canonical Allele Identifier: PA093151
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 344097
ClinVar RCV Id: RCV000371428 RCV003333978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Gly143Asp
CA2692513
NM_000055.4:c.428G>A