Canonical Allele Identifier: PA2829959818
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 430062
ClinVar RCV Id: RCV000494066 RCV000813390 RCV002469176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066264.4:p.Met84Arg
CA5497200
NM_020984.4:c.251T>G