ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826565330
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
187052
ClinVar RCV Id:
RCV000166739
RCV000417885
RCV000430982
RCV000434903
RCV000426124
RCV000441262
RCV000444147
RCV000420162
RCV000432709
RCV000420721
RCV000435516
RCV000424608
RCV000425235
RCV000433509
RCV000443587
RCV001850353
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263689.1:p.Tyr124Asp
CA000239
NM_001276760.3:c.370T>G