Canonical Allele Identifier: PA2826566082
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 132973
ClinVar RCV Id: RCV000119375 RCV000486480 RCV000633378 RCV000774785 RCV003987365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.His257Tyr
CA000474
NM_001276760.3:c.769C>T