Allele Registry

Canonical Allele Identifier: PA2829959774

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000331340

RCV000606672

RCV000698479

ClinVar Variation:

279754

HGVS (amino-acid)	Matching Registered Transcripts
NP_066264.4:p.Val18Met	CA5497135 NM_020984.4:c.52G>A