Canonical Allele Identifier: PA110581
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 13788
ClinVar RCV Id: RCV000014798
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003457.1:p.Gln40Pro
CA123469
NM_003466.4:c.119A>C