Canonical Allele Identifier: PA104869
Gene: WRAP53 HGNC NCBI
ClinVar RCV:
RCV000023967
ClinVar Variation:
30976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.His376Tyr
CA342771
NM_001143990.2:c.1126C>T