Canonical Allele Identifier: PA2826567468
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376677
ClinVar RCV Id: RCV000420150 RCV000421817 RCV000426067 RCV000427353 RCV000426772 RCV000432482 RCV000433292 RCV000437438 RCV000438006 RCV000443517 RCV000444136 RCV001056029 RCV002429350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Val235Ala
CA16603091
NM_001276761.3:c.704T>C