Canonical Allele Identifier: PA2826560436
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2695282
ClinVar RCV Id: RCV003509905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Asp18Gly
CA397846305
NM_001276696.3:c.53A>G