ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825363999
Gene: SUOX
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1811837
ClinVar RCV Id:
RCV002510256
RCV002571586
RCV002571587
RCV003971303
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001027558.1:p.His118Tyr
CA6620963
NM_001032386.2:c.352C>T