Allele Registry

Canonical Allele Identifier: PA2829961305

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019066

ClinVar Variation:

17514

HGVS (amino-acid)	Matching Registered Transcripts
NP_066266.4:p.Arg302Cys	CA257999 NM_020986.4:c.904C>T