Canonical Allele Identifier: PA2573280982
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507306
ClinVar RCV Id: RCV002009424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Arg267Cys
CA8175389
NM_021615.5:c.799C>T