Canonical Allele Identifier: PA2825854443
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17515
ClinVar RCV Id: RCV000019067 RCV001813998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136405.2:p.Ile254Thr
CA258002
NM_001142933.2:c.761T>C