Canonical Allele Identifier: PA2825364288
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2097207
ClinVar RCV Id: RCV003016575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Leu423Pro
CA6621138
NM_001032386.2:c.1268T>C