Canonical Allele Identifier: PA2826567834
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142003
ClinVar RCV Id: RCV000130776 RCV000254695 RCV000663262 RCV000991145 RCV000586942 RCV002225434 RCV003149902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly321Ala
CA000029
NM_001276761.3:c.962G>C