Allele Registry

Canonical Allele Identifier: PA3057587559

Gene: BCHE HGNC NCBI

ClinVar Allele:

3941963

ClinVar RCV:

RCV005303403

ClinVar Variation:

3823374

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Leu327His	CA355111665 NM_000055.4:c.980T>A