Canonical Allele Identifier: PA122149
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12352
ClinVar RCV Id: RCV000013145 RCV000013146 RCV000464372 RCV000579519 RCV000785491 RCV001270276 RCV001562247 RCV003996089 RCV004018617
ClinVar Variation Id: 406598
ClinVar RCV Id: RCV000465003 RCV004022606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Arg117Ser
CA000392
NM_001126116.1:c.351G>T
CA16615944
NM_001126116.1:c.351G>C