Canonical Allele Identifier: PA2825604569
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3148268
ClinVar RCV Id: RCV004440172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Arg213_Tyr220del
CA2825002658
NM_001126113.3:c.637_660del