Canonical Allele Identifier: PA2825537116
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2158751
ClinVar RCV Id: RCV003069925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Gly310Val
CA100000582
NM_001099403.2:c.929G>T