Canonical Allele Identifier: PA2826564222
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 634680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Asp100Tyr
CA397837654
NM_001276699.3:c.298G>T