Canonical Allele Identifier: PA891865357
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13805
ClinVar RCV Id: RCV000014816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003981.3:p.Arg71Thr
CA123481
NM_003990.5:c.212G>C