Canonical Allele Identifier: PA2829961150
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066266.4:p.Ile187Thr
CA257996
NM_020986.4:c.560T>C