Canonical Allele Identifier: PA2741979298
Gene: PRDM13 HGNC NCBI
ClinVar RCV:
RCV003821443
ClinVar Variation:
2968317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067633.2:p.Trp140Arg
CA365115026
NM_021620.4:c.418T>C
CA365115028
NM_021620.4:c.418T>A