Canonical Allele Identifier: PA2829961523
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_066266.4:p.Thr456Ile
CA376747746
NM_020986.4:c.1367C>T