Canonical Allele Identifier: PA2580428573
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2082569
ClinVar RCV Id: RCV003007309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Gly238Asp
CA8175417
NM_021615.5:c.713G>A