Canonical Allele Identifier: PA2580138914
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2016008
ClinVar RCV Id: RCV002846642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Asn161Lys
CA385283972
NM_001032387.2:c.483T>G
CA385283974
NM_001032387.2:c.483T>A