Canonical Allele Identifier: PA2829960669
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 461451
ClinVar RCV Id: RCV000553566
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066265.4:p.Pro434Ser
CA5497585
NM_020985.4:c.1300C>T