Canonical Allele Identifier: PA2825537143
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 643837
ClinVar RCV Id: RCV000797631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Gly359Ser
CA357398081
NM_001099403.2:c.1075G>A