Canonical Allele Identifier: PA2825145142
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1039405
ClinVar RCV Id: RCV002254631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Gln501Lys
CA385297474
NM_000456.3:c.1501C>A