Canonical Allele Identifier: PA2825364383
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1039405
ClinVar RCV Id: RCV002254631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Gln501Lys
CA385297474
NM_001032386.2:c.1501C>A