Canonical Allele Identifier: PA2826565568
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 984966
ClinVar RCV Id: RCV001265630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asn171_Arg174del
CA1139665122
NM_001276760.3:c.511_522del