Canonical Allele Identifier: PA2829496289
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3144740
ClinVar RCV Id: RCV004441597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Lys267Arg
CA5548171
NM_004273.5:c.800A>G