Allele Registry

Canonical Allele Identifier: PA2825853840

Gene: CHAT HGNC NCBI

ClinVar RCV:

RCV000019063

ClinVar Variation:

17511

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136401.2:p.Leu92Pro	CA257990 NM_001142929.2:c.275T>C