Canonical Allele Identifier: PA108074
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 5075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Leu200Arg
CA117249
NM_021615.5:c.599T>G