Canonical Allele Identifier: PA2825364201
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2108628
ClinVar RCV Id: RCV003029525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Asp324Glu
CA6621071
NM_001032386.2:c.972C>A
CA385290097
NM_001032386.2:c.972C>G