Allele Registry

Canonical Allele Identifier: PA2580104328

Gene: BCHE HGNC NCBI

ClinVar Allele:

2398507

ClinVar RCV:

RCV002778981

ClinVar Variation:

2407567

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Asp419Val	CA87410314 NM_000055.4:c.1256A>T