Canonical Allele Identifier: PA2826561417
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376653
ClinVar RCV Id: RCV000419533 RCV000420945 RCV000421561 RCV000420239 RCV000422393 RCV000430463 RCV000428988 RCV000429799 RCV000431805 RCV000434651 RCV000437240 RCV000439247 RCV000440059 RCV000445070 RCV000445103 RCV000690948 RCV000782360 RCV004022239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg210Met
CA16603070
NM_001276696.3:c.629G>T