Allele Registry

Canonical Allele Identifier: PA2825854349

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019058

RCV001092479

ClinVar Variation:

17506

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136405.2:p.Pro129Ala	CA257975 NM_001142933.2:c.385C>G