Canonical Allele Identifier: PA337822
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216468
ClinVar RCV Id: RCV000198322 RCV002354562
ClinVar Variation Id: 480766
ClinVar RCV Id: RCV000566652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Val158Leu
CA337814
NM_001126118.1:c.472G>T
CA397840544
NM_001126118.1:c.472G>C