Canonical Allele Identifier: PA2741854905
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2631749
ClinVar RCV Id: RCV004531572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291498.1:p.Ser92Ile
CA378257698
NM_001304569.2:c.275G>T