Canonical Allele Identifier: PA2825364247
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1475773
ClinVar RCV Id: RCV001976498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Val367Leu
CA385291026
NM_001032386.2:c.1099G>C
CA385291028
NM_001032386.2:c.1099G>T