Canonical Allele Identifier: PA2825606788
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376630
ClinVar RCV Id: RCV000417617 RCV000425579 RCV000425862 RCV000428739 RCV000435274 RCV000435918 RCV000441916 RCV000442239 RCV000459042 RCV000480700 RCV000785496 RCV004022227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Leu111Pro
CA16603049
NM_001126114.3:c.332T>C