Allele Registry

Canonical Allele Identifier: PA093198

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV000014132

ClinVar Variation:

13228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Leu335Pro	CA122971 NM_000055.4:c.1004T>C