Allele Registry

Canonical Allele Identifier: PA2825854558

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV001916006

ClinVar Variation:

1406810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136405.2:p.Val379Leu	CA376742878 NM_001142933.2:c.1135G>C CA376742881 NM_001142933.2:c.1135G>T