Allele Registry

Canonical Allele Identifier: PA093338

Gene: BCHE HGNC NCBI

ClinVar RCV:

RCV000014131

ClinVar Variation:

13227

HGVS (amino-acid)	Matching Registered Transcripts
NP_000046.1:p.Tyr156Cys	CA122970 NM_000055.4:c.467A>G