Canonical Allele Identifier: PA2825145135
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2105317
ClinVar RCV Id: RCV003023391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Ala495Gly
CA385297325
NM_000456.3:c.1484C>G