Allele Registry

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Canonical Allele Identifier: PA2826562096

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019369

ClinVar RCV Id: RCV001318797

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Thr52Ser	CA397840130 NM_001276697.3:c.155C>G CA397840132 NM_001276697.3:c.154A>T