Canonical Allele Identifier: PA2825537151
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497391
ClinVar RCV Id: RCV001996057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Leu370Pro
CA357398303
NM_001099403.2:c.1109T>C