Allele Registry

Canonical Allele Identifier: PA3057550855

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV004965205

ClinVar Variation:

3480089

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Gly381Val	CA2692364 NM_000055.4:c.1142G>T