Allele Registry

Canonical Allele Identifier: PA2573094197

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019066

ClinVar Variation:

17514

HGVS (amino-acid)	Matching Registered Transcripts
NP_065574.4:p.Arg420Cys	CA257999 NM_020549.5:c.1258C>T