Canonical Allele Identifier: PA2825537085
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 217865
ClinVar RCV Id: RCV000201931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Phe261Leu
CA279633
NM_001099403.2:c.781T>C
CA357395212
NM_001099403.2:c.783C>A
CA357395213
NM_001099403.2:c.783C>G