Canonical Allele Identifier: PA2826563042
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376570
ClinVar RCV Id: RCV000417611 RCV000420420 RCV000420646 RCV000425621 RCV000428308 RCV000426275 RCV000427846 RCV000428520 RCV000433667 RCV000436945 RCV000439156 RCV000437617 RCV000439650 RCV000442242 RCV000444511 RCV000492644 RCV001060393 RCV001352918 RCV004022203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Cys17Ser
CA16602996
NM_001276698.3:c.49T>A
CA397841431
NM_001276698.3:c.50G>C
CA645588953
NM_001276698.3:c.48_49delinsTA
CA2695202323
NM_001276698.3:c.50_51delinsCT