Canonical Allele Identifier: PA658679108
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Gly389Arg
CA397830162
NM_001126112.3:c.1165G>A
CA397830168
NM_001126112.3:c.1165G>C