Canonical Allele Identifier: PA2826564449
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332597
ClinVar RCV Id: RCV001805643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Pro142Ala
CA397836355
NM_001276699.3:c.424C>G