Allele Registry

Canonical Allele Identifier: PA2829959822

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019058

RCV001092479

ClinVar Variation:

17506

HGVS (amino-acid)	Matching Registered Transcripts
NP_066264.4:p.Pro93Ala	CA257975 NM_020984.4:c.277C>G