Canonical Allele Identifier: PA2825537152
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 862030
ClinVar RCV Id: RCV001068667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Ala372Thr
CA100000727
NM_001099403.2:c.1114G>A