Allele Registry

Canonical Allele Identifier: PA2829959821

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019063

ClinVar Variation:

17511

HGVS (amino-acid)	Matching Registered Transcripts
NP_066264.4:p.Leu92Pro	CA257990 NM_020984.4:c.275T>C