Canonical Allele Identifier: PA2826565696
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 219759
ClinVar RCV Id: RCV000204217 RCV000424345 RCV000424462 RCV000430896 RCV000433956 RCV000432845 RCV000433328 RCV000445176 RCV000418073 RCV000445265 RCV000423238 RCV000425587 RCV000435222 RCV000440475 RCV000441597 RCV000492197 RCV004020511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Tyr195Asp
CA348450
NM_001276760.3:c.583T>G