Canonical Allele Identifier: PA122138
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12351
ClinVar Variation Id: 237944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro72Arg
CA000072
NM_001126112.3:c.215C>G
CA10583683
NM_001126112.3:c.215_216delinsGT