Canonical Allele Identifier: PA2829479391
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098640
ClinVar RCV Id: RCV003019241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003978.3:p.Val65Ala
CA378257726
NM_003987.5:c.194T>C