Canonical Allele Identifier: PA2825364060
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 957842
ClinVar RCV Id: RCV002254604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Pro162Leu
CA385283993
NM_001032386.2:c.485C>T