Canonical Allele Identifier: PA123470
Gene: PAX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 13788
ClinVar RCV Id: RCV000014798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039247.1:p.Gln40Pro
CA123469
NM_013953.4:c.119A>C