Canonical Allele Identifier: PA2825537145
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920774
ClinVar RCV Id: RCV002604250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Ser360Ile
CA357398104
NM_001099403.2:c.1079G>T