Canonical Allele Identifier: PA107989
Gene: CHST6 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Cys102Gly
CA250520
NM_021615.5:c.304T>G