Canonical Allele Identifier: PA2825364199
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 3172135
ClinVar RCV Id: RCV004461077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Cys317Phe
CA6621069
NM_001032386.2:c.950G>T