Canonical Allele Identifier: PA2825145027
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1475773
ClinVar RCV Id: RCV001976498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Val367Leu
CA385291026
NM_000456.3:c.1099G>C
CA385291028
NM_000456.3:c.1099G>T