Canonical Allele Identifier: PA2580138971
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2108628
ClinVar RCV Id: RCV003029525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Asp324Glu
CA6621071
NM_001032387.2:c.972C>A
CA385290097
NM_001032387.2:c.972C>G