Allele Registry

Canonical Allele Identifier: PA645501997

Gene: ACHE HGNC NCBI

ClinVar RCV:

RCV000020001

ClinVar Variation:

18335

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289551.1:p.His353Asn	CA128044 NM_001302622.2:c.1057C>A