Canonical Allele Identifier: PA2825537109
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1400823
ClinVar RCV Id: RCV001896772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Glu299Gln
CA357395586
NM_001099403.2:c.895G>C