Canonical Allele Identifier: PA108086
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 5078
ClinVar RCV Id: RCV000005383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Leu276Pro
CA250522
NM_021615.5:c.827T>C