Canonical Allele Identifier: PA2826559652
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376620
ClinVar RCV Id: RCV000419550 RCV000418858 RCV000421371 RCV000423525 RCV000424140 RCV000426409 RCV000429158 RCV000428127 RCV000429834 RCV000433822 RCV000434462 RCV000436566 RCV000438380 RCV000439382 RCV000442092 RCV000442140 RCV000633400 RCV002356516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ile156Met
CA16603040
NM_001276695.3:c.468C>G