Canonical Allele Identifier: PA2825854635
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 461451
ClinVar RCV Id: RCV000553566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136405.2:p.Pro470Ser
CA5497585
NM_001142933.2:c.1408C>T