Canonical Allele Identifier: PA2825854424
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136405.2:p.Ile223Thr
CA257996
NM_001142933.2:c.668T>C