Canonical Allele Identifier: PA108248
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 5077
ClinVar RCV Id: RCV000005382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Tyr110Cys
CA250521
NM_021615.5:c.329A>G