Canonical Allele Identifier: PA167857
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142241
ClinVar RCV Id: RCV000131246 RCV000420497 RCV000437502 RCV000438874 RCV000439985 RCV000440358 RCV000445113 RCV000427275 RCV000429077 RCV000430131 RCV000421887 RCV000419499 RCV000419850 RCV000421647 RCV000429319 RCV000431473 RCV000724753 RCV001857457 RCV002288647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Arg117Lys
CA000391
NM_001126116.1:c.350G>A