Canonical Allele Identifier: PA2825854932
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17513
ClinVar RCV Id: RCV000019065 RCV000235033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136406.2:p.Ile187Thr
CA257996
NM_001142934.2:c.560T>C