Canonical Allele Identifier: PA2825854151
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1988713
ClinVar RCV Id: RCV002781438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136401.2:p.Val449Met
CA5497598
NM_001142929.2:c.1345G>A