Canonical Allele Identifier: PA2829960665
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 566556
ClinVar RCV Id: RCV000686399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066265.4:p.Val433Leu
CA376747149
NM_020985.4:c.1297G>T
CA376747152
NM_020985.4:c.1297G>C