Canonical Allele Identifier: PA2825602028
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679228
ClinVar RCV Id: RCV003464698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro322Arg
CA397835872
NM_001126112.3:c.965C>G