Allele Registry

Canonical Allele Identifier: PA2825855028

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019066

ClinVar Variation:

17514

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136406.2:p.Arg302Cys	CA257999 NM_001142934.2:c.904C>T