Canonical Allele Identifier: PA2826561484
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485034
ClinVar RCV Id: RCV000563029 RCV000663222 RCV002526892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Asp220Val
CA397837621
NM_001276696.3:c.659A>T
CA645588489
NM_001276696.3:c.659_660delinsTT