Canonical Allele Identifier: PA916072830
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 652876
ClinVar RCV Id: RCV000808533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064611.3:p.Gln216Leu
CA2982296
NM_020226.4:c.647A>T