Canonical Allele Identifier: PA122198
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12359
ClinVar RCV Id: RCV000013154 RCV000013153 RCV000417576 RCV000422867 RCV000423921 RCV000130168 RCV000418653 RCV000435867 RCV000421750 RCV000426907 RCV000430665 RCV000433125 RCV000441622 RCV000426268 RCV000428255 RCV000434173 RCV000436527 RCV000444801 RCV000559355 RCV000429321 RCV000436959 RCV000438965 RCV000785290 RCV000441398 RCV001255673 RCV002288485 RCV002496336 RCV003114189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Ser241Phe
CA000359
NM_001126113.3:c.722C>T
CA645588606
NM_001126113.3:c.722_723delinsTT