Canonical Allele Identifier: PA107912
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2736373
ClinVar RCV Id: RCV003506579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Arg211Gln
CA8175442
NM_021615.5:c.632G>A