Canonical Allele Identifier: PA2829479710
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_003979.2:p.Arg59Trp
CA378257683
NM_003988.5:c.175C>T