Canonical Allele Identifier: PA2825536986
Gene: PRDM8 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092873.1:p.Ile40Val
CA2982133
NM_001099403.2:c.118A>G