Allele Registry

Canonical Allele Identifier: PA2825854032

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019059

ClinVar Variation:

17507

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136401.2:p.Glu323Lys	CA257978 NM_001142929.2:c.967G>A