Canonical Allele Identifier: PA2580138997
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2185548
ClinVar RCV Id: RCV002596201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg376His
CA385291207
NM_001032387.2:c.1127G>A