Canonical Allele Identifier: PA2499235853
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1037699
ClinVar RCV Id: RCV002254629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ala314Gly
CA385289675
NM_001032387.2:c.941C>G