Canonical Allele Identifier: PA2580139033
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2105317
ClinVar RCV Id: RCV003023391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ala495Gly
CA385297325
NM_001032387.2:c.1484C>G