Canonical Allele Identifier: PA2829746144
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 13788
ClinVar RCV Id: RCV000014798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039246.1:p.Gln40Pro
CA123469
NM_013952.4:c.119A>C