Allele Registry

Canonical Allele Identifier: PA2829961369

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000180671

RCV000988358

ClinVar Variation:

199157

HGVS (amino-acid)	Matching Registered Transcripts
NP_066266.4:p.Val343Met	CA203779 NM_020986.4:c.1027G>A