Canonical Allele Identifier: PA2826564009
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127817
ClinVar RCV Id: RCV000115728 RCV000419908 RCV000417813 RCV000418414 RCV000421548 RCV000426684 RCV000428029 RCV000429595 RCV000439186 RCV000434383 RCV000436065 RCV000439843 RCV001377420 RCV002288599 RCV002288598 RCV003997297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Leu35Phe
CA000278
NM_001276699.3:c.103C>T