Canonical Allele Identifier: PA2825537110
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488956
ClinVar RCV Id: RCV001978183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Ser301Gly
CA357396593
NM_001099403.2:c.901A>G