Canonical Allele Identifier: PA110572
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 13786
ClinVar RCV Id: RCV000014796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003457.1:p.Cys57Tyr
CA123465
NM_003466.4:c.170G>A