Canonical Allele Identifier: PA2829960667
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 461450
ClinVar RCV Id: RCV000540541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066265.4:p.Val433Gly
CA376747159
NM_020985.4:c.1298T>G