Allele Registry

Canonical Allele Identifier: PA2741809139

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV003384850

ClinVar Variation:

2620630

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Phe365Leu	CA2692374 NM_000055.4:c.1095C>G CA355111418 NM_000055.4:c.1095C>A CA355111423 NM_000055.4:c.1093T>C