Allele Registry

Canonical Allele Identifier: PA2829961179

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019067

RCV001813998

ClinVar Variation:

17515

HGVS (amino-acid)	Matching Registered Transcripts
NP_066266.4:p.Ile218Thr	CA258002 NM_020986.4:c.653T>C