Allele Registry

Canonical Allele Identifier: PA2829961150

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019065

RCV000235033

ClinVar Variation:

17513

HGVS (amino-acid)	Matching Registered Transcripts
NP_066266.4:p.Ile187Thr	CA257996 NM_020986.4:c.560T>C