Canonical Allele Identifier: PA2826559700
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376682
ClinVar RCV Id: RCV000418952 RCV000419588 RCV000421235 RCV000421916 RCV000424047 RCV000428672 RCV000426974 RCV000429233 RCV000429897 RCV000431494 RCV000434394 RCV000436627 RCV000439588 RCV000438926 RCV000443993 RCV000443853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Tyr166Phe
CA16603096
NM_001276695.3:c.497A>T