Canonical Allele Identifier: PA1139729461
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 915464
ClinVar RCV Id: RCV001170073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054698.1:p.Ser79Phe
CA348302717
NM_013992.4:c.236C>T