Canonical Allele Identifier: PA2826562499
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376642
ClinVar RCV Id: RCV000421997 RCV000426679 RCV000427094 RCV000427714 RCV000432228 RCV000432977 RCV000433428 RCV000435645 RCV000437941 RCV000439725 RCV000442821 RCV000443572 RCV000444293 RCV000522600 RCV000562528 RCV000633344 RCV000785527 RCV004022233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro119Ser
CA16603059
NM_001276697.3:c.355C>T