Canonical Allele Identifier: PA2826561939
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376609
ClinVar RCV Id: RCV000419091 RCV000418067 RCV000419301 RCV000422109 RCV000422797 RCV000424599 RCV000424807 RCV000427824 RCV000429415 RCV000430449 RCV000433706 RCV000434154 RCV000433494 RCV000435925 RCV000434865 RCV000440508 RCV000440898 RCV000445154 RCV000444321 RCV000564826 RCV000695193 RCV001575036 RCV004022218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His20Asn
CA16603030
NM_001276697.3:c.58C>A