Canonical Allele Identifier: PA169232
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142714
ClinVar Variation Id: 634770
ClinVar Variation Id: 1757269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Met237Ile
CA000349
NM_001126112.3:c.711G>A
CA287488024
NM_001126112.3:c.711G>T
CA287488027
NM_001126112.3:c.711G>C