Canonical Allele Identifier: PA2829952051
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066264.4:p.Ile218Thr
CA258002
NM_020984.4:c.653T>C