Canonical Allele Identifier: PA2826559031
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12351
ClinVar RCV Id: RCV000013144 RCV000034639 RCV000079202 RCV000132165 RCV000144668 RCV000300782 RCV001255631 RCV002225263 RCV002496335 RCV002510562
ClinVar Variation Id: 237944
ClinVar RCV Id: RCV000233585 RCV000780780 RCV002288913 RCV001524923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro33Arg
CA000072
NM_001276695.3:c.98C>G
CA10583683
NM_001276695.3:c.98_99delinsGT