Canonical Allele Identifier: PA2829960213
Gene: CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 17506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066265.4:p.Pro93Ala
CA257975
NM_020985.4:c.277C>G