Canonical Allele Identifier: PA2829961539
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 194108
ClinVar RCV Id: RCV000174391 RCV002516629 RCV000531062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066266.4:p.Val473Met
CA239932
NM_020986.4:c.1417G>A