Canonical Allele Identifier: PA2826565398
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376569
ClinVar RCV Id: RCV000423829 RCV000424063 RCV000423447 RCV000425950 RCV000424490 RCV000429162 RCV000429805 RCV000431923 RCV000435143 RCV000434780 RCV000440706 RCV000440448 RCV000442295 RCV000445093 RCV000445073 RCV001244047 RCV002348142 RCV004022202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Cys137Phe
CA16602995
NM_001276760.3:c.410G>T
CA645588949
NM_001276760.3:c.410_411delinsTT