Canonical Allele Identifier: PA2825619035
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1471105
ClinVar RCV Id: RCV001995379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Pro270Leu
CA397836130
NM_001126118.1:c.809C>T