Canonical Allele Identifier: PA2826567232
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376636
ClinVar RCV Id: RCV000420529 RCV000422293 RCV000424589 RCV000427086 RCV000429783 RCV000432913 RCV000435309 RCV000436968 RCV000437739 RCV000442354 RCV000442966 RCV000443369 RCV002509381 RCV002524697 RCV004022231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Met198Lys
CA001811
NM_001276761.3:c.593T>A