Allele Registry

Canonical Allele Identifier: PA645487570

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV000265515

ClinVar Variation:

344092

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Gly393Val	CA10615760 NM_000055.4:c.1178G>T