Canonical Allele Identifier: PA2825854146
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2301069
ClinVar RCV Id: RCV002883348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136401.2:p.Arg448Pro
CA376747546
NM_001142929.2:c.1343G>C