Allele Registry

Canonical Allele Identifier: PA093168

Gene: BCHE HGNC NCBI

ClinVar Allele:

227254

ClinVar RCV:

RCV000490265

ClinVar Variation:

225301

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