Allele Registry

Canonical Allele Identifier: PA2829959817

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV003324209

ClinVar Variation:

2577132

HGVS (amino-acid)	Matching Registered Transcripts
NP_066264.4:p.Met84Thr	CA206625625 NM_020984.4:c.251T>C