Canonical Allele Identifier: PA2826561139
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 826165
ClinVar RCV Id: RCV001024853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg163Pro
CA397840404
NM_001276696.3:c.488G>C
CA645588790
NM_001276696.3:c.488_489delinsCG