Canonical Allele Identifier: PA2825145122
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1420987
ClinVar RCV Id: RCV001923635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Glu478Asp
CA385294854
NM_000456.3:c.1434G>C
CA385294859
NM_000456.3:c.1434G>T