Canonical Allele Identifier: PA2826566918
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186451
ClinVar RCV Id: RCV000166045 RCV000418577 RCV000419236 RCV000422335 RCV000429854 RCV000437356 RCV000430568 RCV000441417 RCV000424233 RCV000430147 RCV000433025 RCV000438398 RCV000461158 RCV000255616 RCV000421421 RCV000432068 RCV000435778 RCV000441274 RCV002288754 RCV001354219 RCV003128588 RCV003407616 RCV003474872 RCV003995473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys137Tyr
CA000254
NM_001276761.3:c.410G>A