Allele Registry

Canonical Allele Identifier: PA093073

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV000014102

RCV000277104

RCV001092437

RCV003415696

ClinVar Variation:

13215

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Asp98Gly	CA122963 NM_000055.4:c.293A>G