Canonical Allele Identifier: PA645387729
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309833
ClinVar RCV Id: RCV000351081 RCV002522240 RCV003488520 RCV003920288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Arg76Ser
CA6620904
NM_000456.3:c.228G>T
CA385279967
NM_000456.3:c.228G>C