Canonical Allele Identifier: PA2826562500
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 232497
ClinVar RCV Id: RCV000214784 RCV000419043 RCV000440687 RCV000429345 RCV000430442 RCV000434963 RCV000417969 RCV000423023 RCV000421915 RCV000424153 RCV000428205 RCV000439555 RCV000433311 RCV000443824 RCV000785311 RCV001042706 RCV001374441 RCV001541668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro119Leu
CA10580915
NM_001276697.3:c.356C>T