Canonical Allele Identifier: PA093168
Gene: BCHE HGNC NCBI

Linked Data

ClinVar Variation Id: 225301
ClinVar RCV Id: RCV000490265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000046.1:p.Gly393Arg
CA2692359
NM_000055.4:c.1177G>C
CA355111225
NM_000055.4:c.1177G>A