Allele Registry

Canonical Allele Identifier: PA2829938178

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019063

ClinVar Variation:

17511

HGVS (amino-acid)	Matching Registered Transcripts
NP_065574.4:p.Leu210Pro	CA257990 NM_020549.5:c.629T>C