Allele Registry

Canonical Allele Identifier: PA3057550860

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV004965208

ClinVar Variation:

3480092

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Ala430Asp	CA2692342 NM_000055.4:c.1289C>A