Canonical Allele Identifier: PA2826566138
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406589
ClinVar RCV Id: RCV000473016 RCV001805064 RCV002289599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asn272Ser
CA16615690
NM_001276760.3:c.815A>G