Allele Registry

Canonical Allele Identifier: PA2825854847

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV003324209

ClinVar Variation:

2577132

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136406.2:p.Met84Thr	CA206625625 NM_001142934.2:c.251T>C