Canonical Allele Identifier: PA2825854157
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 958996
ClinVar RCV Id: RCV001232267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136401.2:p.Thr456Ile
CA376747746
NM_001142929.2:c.1367C>T