Canonical Allele Identifier: PA891865361
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_003981.3:p.Gly76Ser
CA256966
NM_003990.5:c.226G>A