Allele Registry

Canonical Allele Identifier: PA916047039

Gene: ACHE HGNC NCBI

ClinVar RCV:

RCV000020001

ClinVar Variation:

18335

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354847.1:p.His420Asn	CA128044 NM_001367918.1:c.1258C>A