Allele Registry

Canonical Allele Identifier: PA2829952262

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019061

RCV002274884

ClinVar Variation:

17509

HGVS (amino-acid)	Matching Registered Transcripts
NP_066264.4:p.Arg364Gly	CA257984 NM_020984.4:c.1090A>G