Canonical Allele Identifier: PA2826561477
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_001263625.1:p.Glu219Lys
CA000406
NM_001276696.3:c.655G>A
CA645588496
NM_001276696.3:c.654_655delinsAA