Canonical Allele Identifier: PA2829961535
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1038322
ClinVar RCV Id: RCV001341615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066266.4:p.Val466Met
CA5497607
NM_020986.4:c.1396G>A