Canonical Allele Identifier: PA2826565634
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12383
ClinVar RCV Id: RCV000013183 RCV000423167 RCV000424238 RCV000418406 RCV000432708 RCV000422874 RCV000436486 RCV000425801 RCV000428157 RCV000430581 RCV000433786 RCV000441285 RCV000444276 RCV000445060 RCV000472593 RCV000443214 RCV000785481 RCV000417473 RCV000425300 RCV000429097 RCV000435597 RCV000441465 RCV003162249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Tyr181Ser
CA000314
NM_001276760.3:c.542A>C