Canonical Allele Identifier: PA2580193309
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098640
ClinVar RCV Id: RCV003019241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291498.1:p.Val96Ala
CA378257726
NM_001304569.2:c.287T>C