Canonical Allele Identifier: PA2826567158
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 161397
ClinVar RCV Id: RCV000161032 RCV000148907 RCV000213056 RCV000411498 RCV001002287 RCV000989715 RCV001798464 RCV003905279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro183Leu
CA000317
NM_001276761.3:c.548C>T
CA645588718
NM_001276761.3:c.547_548delinsTT