Allele Registry

Canonical Allele Identifier: PA2573277827

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV001916006

ClinVar Variation:

1406810

HGVS (amino-acid)	Matching Registered Transcripts
NP_065574.4:p.Val461Leu	CA376742878 NM_020549.5:c.1381G>C CA376742881 NM_020549.5:c.1381G>T