Canonical Allele Identifier: PA2825862050
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 392640
ClinVar RCV Id: RCV000426413 RCV000767151 RCV002418337 RCV003942461
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Pro359Ser
CA8355254
NM_001143992.2:c.1075C>T