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