Canonical Allele Identifier: PA2499288126
Gene: PRDM13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002070
ClinVar RCV Id: RCV001298444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067633.2:p.Pro19Ser
CA365113140
NM_021620.4:c.55C>T