Canonical Allele Identifier: PA2829961062
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 128726
ClinVar RCV Id: RCV000116699 RCV000552676 RCV000676664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066266.4:p.Leu125Phe
CA152358
NM_020986.4:c.373C>T