Canonical Allele Identifier: PA2499288132
Gene: PRDM13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016645
ClinVar RCV Id: RCV001315680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067633.2:p.Trp118Leu
CA143972454
NM_021620.4:c.353G>T