Canonical Allele Identifier: PA2826896255
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13799
ClinVar RCV Id: RCV000014810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291498.1:p.Gly107Ser
CA256966
NM_001304569.2:c.319G>A