Canonical Allele Identifier: PA2499288133
Gene: PRDM13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062409
ClinVar RCV Id: RCV001372121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067633.2:p.Thr124Ala
CA365114193
NM_021620.4:c.370A>G