Canonical Allele Identifier: PA2826560771
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376559
ClinVar RCV Id: RCV000417503 RCV000418582 RCV000425788 RCV000426876 RCV000427781 RCV000428180 RCV000434318 RCV000436707 RCV000435797 RCV000436440 RCV000438861 RCV000444308 RCV000444605 RCV000492398 RCV001203469 RCV004022199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys96Phe
CA16602985
NM_001276696.3:c.287G>T