Canonical Allele Identifier: PA2573174968
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1475773
ClinVar RCV Id: RCV001976498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Val367Leu
CA385291026
NM_001032387.2:c.1099G>C
CA385291028
NM_001032387.2:c.1099G>T