Canonical Allele Identifier: PA2825854339
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 430062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136405.2:p.Met120Arg
CA5497200
NM_001142933.2:c.359T>G