Canonical Allele Identifier: PA2825537077
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046471
ClinVar RCV Id: RCV001351035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Ala248Thr
CA2982320
NM_001099403.2:c.742G>A