Canonical Allele Identifier: PA2826561372
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182936
ClinVar RCV Id: RCV000161035 RCV000222280 RCV000686581 RCV003462110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Met204Thr
CA000365
NM_001276696.3:c.611T>C
CA645588591
NM_001276696.3:c.611_612delinsCA