Canonical Allele Identifier: PA2825854127
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 566556
ClinVar RCV Id: RCV000686399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136401.2:p.Val433Leu
CA376747149
NM_001142929.2:c.1297G>T
CA376747152
NM_001142929.2:c.1297G>C