Canonical Allele Identifier: PA2825138338
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087854
ClinVar RCV Id: RCV003009771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000269.3:p.Ser66Arg
CA378257728
NM_000278.5:c.196A>C
CA378257734
NM_000278.5:c.198C>A
CA378257735
NM_000278.5:c.198C>G