Canonical Allele Identifier: PA2826567379
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12372
ClinVar RCV Id: RCV000013171 RCV000469142 RCV000785553 RCV002399320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Leu218Gln
CA000402
NM_001276761.3:c.653T>A