Canonical Allele Identifier: PA2825854141
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136401.2:p.Arg442His
CA257987
NM_001142929.2:c.1325G>A