Canonical Allele Identifier: PA2829746161
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 13786
ClinVar RCV Id: RCV000014796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039246.1:p.Cys57Tyr
CA123465
NM_013952.4:c.170G>A