Canonical Allele Identifier: PA645435613
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376690
ClinVar RCV Id: RCV000421263 RCV000421924 RCV000423467 RCV000427293 RCV000430039 RCV000430207 RCV000431511 RCV000433051 RCV000437540 RCV000439556 RCV000440245 RCV000444569 RCV000443862 RCV000444596 RCV001025931 RCV001341542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Tyr234Ser
CA16603103
NM_001126114.3:c.701A>C