Allele Registry

Canonical Allele Identifier: PA3057587562

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV005303397

ClinVar Variation:

3823363

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Asp482Glu	CA2692309 NM_000055.4:c.1446T>A CA355110628 NM_000055.4:c.1446T>G