Canonical Allele Identifier: PA2826560768
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376561
ClinVar RCV Id: RCV000417767 RCV000420893 RCV000420220 RCV000423274 RCV000424924 RCV000429841 RCV000430892 RCV000432245 RCV000434979 RCV000435704 RCV000439451 RCV000440498 RCV000441628 RCV000479510 RCV000556410 RCV002289519 RCV002289518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys96Trp
CA16602987
NM_001276696.3:c.288C>G