Canonical Allele Identifier: PA2826565555
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 439319
ClinVar RCV Id: RCV000507226 RCV000566251 RCV001049540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Leu167Ser
CA397840264
NM_001276760.3:c.500T>C