Allele Registry

Canonical Allele Identifier: PA2829938181

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019058

RCV001092479

ClinVar Variation:

17506

HGVS (amino-acid)	Matching Registered Transcripts
NP_065574.4:p.Pro211Ala	CA257975 NM_020549.5:c.631C>G