Allele Registry

Canonical Allele Identifier: PA2829951879

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000116697

RCV000676662

RCV001519257

ClinVar Variation:

128724

HGVS (amino-acid)	Matching Registered Transcripts
NP_066264.4:p.Ala2Thr	CA152352 NM_020984.4:c.4G>A