Allele Registry

Canonical Allele Identifier: PA3057587561

Gene: BCHE HGNC NCBI

ClinVar Allele:

3941941

ClinVar RCV:

RCV005314002

ClinVar Variation:

3823352

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Asp368Val	CA2692373 NM_000055.4:c.1103A>T