Canonical Allele Identifier: PA2826560498
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485023
ClinVar RCV Id: RCV000573116 RCV002304214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro33Ser
CA003069
NM_001276696.3:c.97C>T
CA2838032368
NM_001276696.3:c.97_98delinsAG