Canonical Allele Identifier: PA2829952325
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 649407
ClinVar RCV Id: RCV000804335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066264.4:p.Glu437Lys
CA5497589
NM_020984.4:c.1309G>A