Allele Registry

Canonical Allele Identifier: PA2825854338

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV003324209

ClinVar Variation:

2577132

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136405.2:p.Met120Thr	CA206625625 NM_001142933.2:c.359T>C