Allele Registry

Canonical Allele Identifier: PA2829938165

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV003324209

ClinVar Variation:

2577132

HGVS (amino-acid)	Matching Registered Transcripts
NP_065574.4:p.Met202Thr	CA206625625 NM_020549.5:c.605T>C