Canonical Allele Identifier: PA2573094231
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 844118
ClinVar RCV Id: RCV001046887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065574.4:p.Ala579Thr
CA5497603
NM_020549.5:c.1735G>A