Canonical Allele Identifier: PA645503067
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 436165
ClinVar RCV Id: RCV000502399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039247.1:p.Ser54Cys
CA348303328
NM_013953.4:c.160A>T