Canonical Allele Identifier: PA2580428574
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2367531
ClinVar RCV Id: RCV002992001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Gly238Ser
CA8175419
NM_021615.5:c.712G>A