Allele Registry

Canonical Allele Identifier: PA2580104327

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV002678004

ClinVar Variation:

2219748

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Gly381Ala	CA2692365 NM_000055.4:c.1142G>C