Allele Registry

Canonical Allele Identifier: PA2829959939

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV001916006

ClinVar Variation:

1406810

HGVS (amino-acid)	Matching Registered Transcripts
NP_066264.4:p.Val343Leu	CA376742878 NM_020984.4:c.1027G>C CA376742881 NM_020984.4:c.1027G>T