Canonical Allele Identifier: PA2825854136
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 461452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136401.2:p.Ala439Thr
CA5497591
NM_001142929.2:c.1315G>A