Canonical Allele Identifier: PA2826560749
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376625
ClinVar RCV Id: RCV000419418 RCV000418417 RCV000419619 RCV000421674 RCV000424246 RCV000423130 RCV000428190 RCV000426827 RCV000429087 RCV000429251 RCV000434074 RCV000436453 RCV000436660 RCV000438897 RCV000441520 RCV000443007 RCV000471183 RCV000785521 RCV002356517 RCV004022224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Lys93Arg
CA16603045
NM_001276696.3:c.278A>G