Canonical Allele Identifier: PA645503079
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 426842
ClinVar RCV Id: RCV000490149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039247.1:p.Gly93Ala
CA348302550
NM_013953.4:c.278G>C