Canonical Allele Identifier: PA2826566470
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473030
ClinVar RCV Id: RCV001969440
ClinVar Variation Id: 1775671
ClinVar RCV Id: RCV002405782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Trp14Arg
CA397846498
NM_001276761.3:c.40T>C
CA397846503
NM_001276761.3:c.40T>A