Canonical Allele Identifier: PA2826559070
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182946
ClinVar RCV Id: RCV000161047 RCV000213048 RCV000205955 RCV000989726 RCV001250438 RCV001355900 RCV003965183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro43Leu
CA000080
NM_001276695.3:c.128C>T