Allele Registry

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Canonical Allele Identifier: PA2826560678

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480758

ClinVar RCV Id: RCV000565337

ClinVar Variation Id: 1462102

ClinVar RCV Id: RCV001954182 RCV003339855

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Gly78Arg	CA397844409 NM_001276696.3:c.232G>C CA397844412 NM_001276696.3:c.232G>A