Canonical Allele Identifier: PA2826567700
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12367
ClinVar RCV Id: RCV000232570 RCV001508433 RCV000013166 RCV000013165 RCV000131411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly286Val
CA000516
NM_001276761.3:c.857G>T