Allele Registry

Canonical Allele Identifier: PA093151

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV000371428

RCV003333978

ClinVar Variation:

344097

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