Canonical Allele Identifier: PA2499288134
Gene: PRDM13 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067633.2:p.Glu131Lys
CA143972492
NM_021620.4:c.391G>A