Canonical Allele Identifier: PA2829479398
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333615
ClinVar RCV Id: RCV001808303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003978.3:p.Arg71Gly
CA378257762
NM_003987.5:c.211A>G