Canonical Allele Identifier: PA2826566348
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 858737
ClinVar RCV Id: RCV001064680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser328Thr
CA397831738
NM_001276760.3:c.983G>C