Canonical Allele Identifier: PA2825610152
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3148387
ClinVar RCV Id: RCV004440292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Ala57_Leu62del
CA2825002604
NM_001126115.1:c.168_185del