Allele Registry

Canonical Allele Identifier: PA2741809155

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV003357082

ClinVar Variation:

2604305

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Val496Met	CA355110538 NM_000055.4:c.1486G>A