Canonical Allele Identifier: PA2826564539
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Glu167Asp
CA287486513
NM_001276699.3:c.501A>T
CA397835791
NM_001276699.3:c.501A>C