Allele Registry

Canonical Allele Identifier: PA1139671137

Gene: BCHE HGNC NCBI

ClinVar Allele:

888351

ClinVar RCV:

RCV001146602

ClinVar Variation:

900999

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Ile384Val	CA2692362 NM_000055.4:c.1150A>G