Canonical Allele Identifier: PA915957682
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 623385
ClinVar RCV Id: RCV000761535 RCV001759448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ser463Phe
CA385294306
NM_001032387.2:c.1388C>T