Canonical Allele Identifier: PA2826565141
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376627
ClinVar RCV Id: RCV000420694 RCV000419605 RCV000423393 RCV000422403 RCV000424547 RCV000425633 RCV000427017 RCV000430299 RCV000433243 RCV000433123 RCV000435461 RCV000437675 RCV000437910 RCV000443063 RCV000442106 RCV000442467 RCV004022225 RCV003621532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Lys93Thr
CA16603046
NM_001276760.3:c.278A>C