Canonical Allele Identifier: PA2829459447
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 915464
ClinVar RCV Id: RCV001170073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003457.1:p.Ser79Phe
CA348302717
NM_003466.4:c.236C>T