Canonical Allele Identifier: PA645499741
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 392640
ClinVar RCV Id: RCV000426413 RCV000767151 RCV002418337 RCV003942461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.Pro359Ser
CA8355254
NM_018081.2:c.1075C>T