Canonical Allele Identifier: PA2825614499
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679228
ClinVar RCV Id: RCV003464698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Pro190Arg
CA397835872
NM_001126116.1:c.569C>G