Canonical Allele Identifier: PA123457
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 13782
ClinVar RCV Id: RCV000014792 RCV001133552 RCV001698942 RCV003974824 RCV003430637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003457.1:p.Phe329Leu
CA123456
NM_003466.4:c.985T>C
CA348315655
NM_003466.4:c.987T>G
CA348315657
NM_003466.4:c.987T>A