Canonical Allele Identifier: PA2573069844
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333274
ClinVar RCV Id: RCV001807962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291498.1:p.Arg90Trp
CA378257683
NM_001304569.2:c.268C>T