Canonical Allele Identifier: PA2825145087
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1512644
ClinVar RCV Id: RCV002023141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Glu436Asp
CA385293249
NM_000456.3:c.1308G>C
CA385293266
NM_000456.3:c.1308G>T