Canonical Allele Identifier: PA2825854676
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 194108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136405.2:p.Val509Met
CA239932
NM_001142933.2:c.1525G>A