Canonical Allele Identifier: PA287742
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127815
ClinVar RCV Id: RCV000115726 RCV000423020 RCV000423688 RCV000428854 RCV000444364 RCV000424007 RCV000424716 RCV000427283 RCV000444227 RCV000419735 RCV000555493 RCV000431087 RCV000434379 RCV000436304 RCV000663095 RCV000785312 RCV000419024 RCV000430411 RCV000434725 RCV000435360 RCV000436095 RCV000440222 RCV000441827 RCV002288597 RCV003460828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.His47Tyr
CA000256
NM_001126115.1:c.139C>T
CA645588931
NM_001126115.1:c.138_139delinsTT