Canonical Allele Identifier: PA2825610059
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2687634
ClinVar RCV Id: RCV003484383
ClinVar Variation Id: 3074246
ClinVar RCV Id: RCV004012788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.His47del
CA645588925
NM_001126115.1:c.138_140del
CA2825002607
NM_001126115.1:c.139_141del