Canonical Allele Identifier: PA2825598465
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro4Arg
CA16615964
NM_001126112.3:c.11C>G