Allele Registry

Canonical Allele Identifier: PA3057550853

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV004965211

ClinVar Variation:

3480095

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Asp296Val	CA355111858 NM_000055.4:c.887A>T