Canonical Allele Identifier: PA093198
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 13228
ClinVar RCV Id: RCV000014132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Leu335Pro
CA122971
NM_000055.4:c.1004T>C