Canonical Allele Identifier: PA2825854147
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1444825
ClinVar RCV Id: RCV001955999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136401.2:p.Arg448Cys
CA5497596
NM_001142929.2:c.1342C>T