Canonical Allele Identifier: PA916006456
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12348
ClinVar RCV Id: RCV000013141 RCV000582699 RCV000785291 RCV000792895 RCV000161071 RCV000772122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Glu99Lys
CA000406
NM_001276699.3:c.295G>A
CA645588496
NM_001276699.3:c.294_295delinsAA