Canonical Allele Identifier: PA2829938322
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065574.4:p.Ile305Thr
CA257996
NM_020549.5:c.914T>C