Allele Registry

Canonical Allele Identifier: PA2741809141

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV003242639

ClinVar Variation:

2545443

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Asn369Lys	CA355111387 NM_000055.4:c.1107C>G CA355111388 NM_000055.4:c.1107C>A