Canonical Allele Identifier: PA2825144980
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2108628
ClinVar RCV Id: RCV003029525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Asp324Glu
CA6621071
NM_000456.3:c.972C>A
CA385290097
NM_000456.3:c.972C>G