Canonical Allele Identifier: PA658734149
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 496047
ClinVar RCV Id: RCV000587100 RCV001016639 RCV002289886
ClinVar Variation Id: 528238
ClinVar RCV Id: RCV000633332
ClinVar Variation Id: 821828
ClinVar RCV Id: RCV001016637 RCV002290531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ser9Arg
CA003949
NM_001126114.3:c.27C>G
CA397849245
NM_001126114.3:c.27C>A
CA397849282
NM_001126114.3:c.25A>C