Canonical Allele Identifier: PA2829960317
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066265.4:p.Ile187Thr
CA257996
NM_020985.4:c.560T>C