Canonical Allele Identifier: PA2825364076
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1423640
ClinVar RCV Id: RCV001928979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Val181Leu
CA385284459
NM_001032386.2:c.541G>T
CA385284460
NM_001032386.2:c.541G>C