Canonical Allele Identifier: PA1139673669
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 989295
ClinVar RCV Id: RCV001270791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Gln274His
CA6621051
NM_001032387.2:c.822G>C
CA385288203
NM_001032387.2:c.822G>T