Canonical Allele Identifier: PA2825854669
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 844118
ClinVar RCV Id: RCV001046887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136405.2:p.Ala497Thr
CA5497603
NM_001142933.2:c.1489G>A